0000950123-11-073724.txt : 20110805 0000950123-11-073724.hdr.sgml : 20110805 20110805163748 ACCESSION NUMBER: 0000950123-11-073724 CONFORMED SUBMISSION TYPE: 10-Q PUBLIC DOCUMENT COUNT: 12 CONFORMED PERIOD OF REPORT: 20110630 FILED AS OF DATE: 20110805 DATE AS OF CHANGE: 20110805 FILER: COMPANY DATA: COMPANY CONFORMED NAME: HeartWare International, Inc. CENTRAL INDEX KEY: 0001389072 STANDARD INDUSTRIAL CLASSIFICATION: SURGICAL & MEDICAL INSTRUMENTS & APPARATUS [3841] IRS NUMBER: 980498958 STATE OF INCORPORATION: DE FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 10-Q SEC ACT: 1934 Act SEC FILE NUMBER: 001-34256 FILM NUMBER: 111014687 BUSINESS ADDRESS: STREET 1: 14000 NW 57TH COURT CITY: MIAMI LAKES STATE: FL ZIP: 33014 BUSINESS PHONE: 508-739-0841 MAIL ADDRESS: STREET 1: 205 NEWBURY STREET STREET 2: SUITE 101 CITY: FRAMINGHAM STATE: MA ZIP: 01701 FORMER COMPANY: FORMER CONFORMED NAME: HeartWare LTD DATE OF NAME CHANGE: 20070206 10-Q 1 c18306e10vq.htm FORM 10-Q Form 10-Q
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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-Q
     
þ   Quarterly report pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
For the quarterly period ended June 30, 2011
     
o   Transition report pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
For the transition period from                      to                     
COMMISSION FILE NUMBER: 001-34256
HEARTWARE INTERNATIONAL, INC.
(Exact name of registrant as specified in its charter)
     
Delaware   26-3636023
     
(State of Incorporation)   (I.R.S. Employer Identification No.)
205 Newbury Street, Suite 101
Framingham, Massachusetts 01701
+1 508 739 0950
(Address of principal executive offices)
(Registrant’s telephone number, including area code)
 
Indicate by check mark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15 (d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes þ No o
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). Yes þ No o
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, or a non-accelerated filer or a smaller reporting company. See the definitions of “large accelerated filer”, “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act.
             
Large accelerated filer o   Accelerated filer þ   Non-accelerated filer o   Smaller reporting company o
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes o No þ
Indicate the number of shares outstanding of each of the issuer’s classes of common stock, as of the latest practicable date.
     
Class   Shares Outstanding as of July 27, 2011
     
Common Stock, $0.001 Par Value Per Share   13,925,984
 
 

 

 


 

         
 
       
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 Exhibit 10.35
 Exhibit 31.1
 Exhibit 31.2
 Exhibit 32.1
 Exhibit 32.2
 EX-101 INSTANCE DOCUMENT
 EX-101 SCHEMA DOCUMENT
 EX-101 CALCULATION LINKBASE DOCUMENT
 EX-101 LABELS LINKBASE DOCUMENT
 EX-101 PRESENTATION LINKBASE DOCUMENT
 EX-101 DEFINITION LINKBASE DOCUMENT

 

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References
Unless the context requires otherwise, references in this Quarterly Report on Form 10-Q to:
    “HeartWare,” “the Company,” “HeartWare Group,” “we,” “us” and “our” refer to HeartWare International, Inc. and its consolidated subsidiaries, HeartWare Pty. Limited, HeartWare, Inc., HeartWare GmbH and HeartWare (UK) Limited.
 
    “HeartWare International, Inc.” refers to HeartWare International, Inc., a Delaware corporation incorporated on July 29, 2008.
 
    “HeartWare Pty. Limited” refers to HeartWare Pty. Limited (formerly known as HeartWare Limited), an Australian proprietary corporation originally incorporated on November 26, 2004.
 
    “HeartWare, Inc.” refers to HeartWare, Inc., a Delaware corporation incorporated on April 3, 2003. HeartWare, Inc. was acquired by HeartWare Pty. Limited on January 24, 2005.
 
    “HeartWare GmbH” refers to HeartWare GmbH, a German corporation established on February 19, 2010.
 
    “HeartWare (UK) Limited” refers to HeartWare (UK) Limited, a limited liability corporation established in the United Kingdom on February 19, 2010.
Currency
Unless indicated otherwise in this Quarterly Report on Form 10-Q, all references to “$”, “U.S.$” or “dollars” refer to United States dollars, the lawful currency of the United States of America. References to “AU$” refer to Australian dollars, the lawful currency of the Commonwealth of Australia, and references to “€” or “Euros” means Euros, the single currency of Participating Member States of the European Union.
Trademarks
HEARTWARE®, HVAD® and MVAD®, KRITON® and various company logos are the trademarks of the Company in the United States, Europe, Australia and other countries. All other trademarks and trade names mentioned in this Quarterly Report on Form 10-Q are the property of their respective owners.
Forward-Looking Statements
This Quarterly Report on Form 10-Q contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These forward-looking statements are based on our management’s beliefs, assumptions and expectations and on information currently available to our management. Generally, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “could,” “would,” “expects,” “plans,” “anticipates,” “believes,” “estimates,” “projects,” “predicts,” “potential” and similar expressions intended to identify forward-looking statements, which generally are not historical in nature. All statements that address operating or financial performance, events or developments that we expect or anticipate will occur in the future are forward-looking statements, including without limitation:
    our expectations with respect to regulatory submissions and approvals, such as United States Food & Drug Administration (“FDA”) approval of our premarket approval application for our HeartWare® Ventricular Assist System for a bridge-to-transplant indication;
 
    our expectations with respect to our clinical trials, including enrollment in or completion of our clinical trials;
 
    our expectations with respect to the integrity or capabilities of our intellectual property position;
 
    our ability and plans to commercialize our existing products;
 
    our ability and plans to develop and commercialize new products and the expected features and functionalities and possible benefits of these products; and
 
    our estimates regarding our capital requirements and financial performance, including profitability.

 

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Our management believes that these forward-looking statements are reasonable as and when made. However, you should not place undue reliance on forward-looking statements because they speak only as of the date when made. We do not assume any obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be required by federal securities laws and the rules of the Securities and Exchange Commission (the “SEC”). We may not actually achieve the plans, projections or expectations disclosed in our forward-looking statements, and actual results, developments or events could differ materially from those disclosed in the forward-looking statements. Forward-looking statements are subject to a number of risks and uncertainties, including without limitation those described in Part I, “Item 1A. Risk Factors” in our Annual Report on Form 10-K for the fiscal year ended December 31, 2010 filed with the SEC on February 24, 2011, and those described from time to time in our other filings with the SEC.

 

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PART I. FINANCIAL INFORMATION
ITEM 1.   CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
HEARTWARE INTERNATIONAL, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(unaudited)
                 
    June 30, 2011     December 31, 2010  
ASSETS
               
Current assets:
               
Cash and cash equivalents
  $ 118,843,674     $ 192,148,312  
Short-term investments, net
    79,998,132       21,330,110  
Accounts receivable, net
    15,248,062       19,052,672  
Inventories, net
    22,522,356       15,076,590  
Prepaid expenses and other current assets
    4,659,251       2,406,505  
 
           
 
               
Total current assets
    241,271,475       250,014,189  
 
               
Property, plant and equipment, net
    11,130,352       7,484,022  
Long-term investments, net
          4,005,659  
Other intangible assets, net
    1,785,509       1,595,456  
Deferred financing costs, net
    2,800,497       2,939,149  
Restricted cash
    1,538,429       1,538,429  
 
           
 
               
Total assets
  $ 258,526,262     $ 267,576,904  
 
           
 
               
LIABILITIES AND STOCKHOLDERS’ EQUITY
               
Current liabilities:
               
Accounts payable
  $ 3,336,590     $ 3,889,643  
Accrued expenses and other current liabilities
    8,331,089       7,001,350  
 
           
 
               
Total current liabilities
    11,667,679       10,890,993  
 
               
Convertible senior notes, net
    91,518,710       88,921,557  
 
               
Commitments and contingencies — See Note 16
               
 
               
Stockholders’ equity:
               
Preferred stock — $.001 par value; 5,000,000 shares authorized; no shares issued and outstanding at June 30, 2011 and December 31, 2010
           
Common stock — $.001 par value; 25,000,000 shares authorized; 13,925,984 and 13,878,686 shares issued and outstanding at June 30, 2011 and December 31, 2010, respectively
    13,926       13,879  
Additional paid-in capital
    309,569,724       302,533,344  
Accumulated deficit
    (146,795,591 )     (127,268,545 )
Accumulated other comprehensive loss:
               
Cumulative translation adjustments
    (7,457,261 )     (7,548,706 )
Unrealized gain on investments
    9,075       34,382  
 
           
Total accumulated other comprehensive loss
    (7,448,186 )     (7,514,324 )
 
               
Total stockholders’ equity
    155,339,873       167,764,354  
 
           
 
               
Total liabilities and stockholders’ equity
  $ 258,526,262     $ 267,576,904  
 
           
The accompanying notes are an integral part of these financial statements.

 

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HEARTWARE INTERNATIONAL, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(unaudited)
                                 
    Three Months Ended     Six Months Ended  
    June 30,     June 30,  
    2011     2010     2011     2010  
 
                               
Revenues, net
  $ 20,389,491     $ 9,757,078     $ 38,364,091     $ 20,460,198  
Cost of revenues
    7,913,346       4,293,348       15,508,799       9,973,890  
 
                       
Gross profit
    12,476,145       5,463,730       22,855,292       10,486,308  
 
                               
Operating expenses:
                               
 
                               
Selling, general and administrative
    9,892,325       7,688,379       18,556,413       12,244,801  
Research and development
    10,279,529       7,511,201       19,579,657       12,266,879  
 
                       
Total operating expenses
    20,171,854       15,199,580       38,136,070       24,511,680  
 
                               
Loss from operations
    (7,695,709 )     (9,735,850 )     (15,280,778 )     (14,025,372 )
 
                               
Other income (expense):
                               
 
                               
Foreign exchange gain (loss)
    133,889       (406,486 )     726,214       (773,500 )
Interest expense
    (2,646,558 )     (971 )     (5,252,030 )     (971 )
Investment income, net
    127,902       161,258       295,100       273,479  
Other, net
    (15,552 )           (15,552 )      
 
                       
 
                               
Loss before income taxes
    (10,096,028 )     (9,982,049 )     (19,527,046 )     (14,526,364 )
Provision for income taxes
                       
 
                       
 
                               
Net loss
  $ (10,096,028 )   $ (9,982,049 )   $ (19,527,046 )   $ (14,526,364 )
 
                       
 
                               
Net loss per common share — basic and diluted
  $ (0.73 )   $ (0.73 )   $ (1.40 )   $ (1.09 )
 
                       
 
                               
Weighted average shares outstanding — basic and diluted
    13,923,258       13,682,734       13,911,993       13,322,531  
 
                       
The accompanying notes are an integral part of these financial statements.

 

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HEARTWARE INTERNATIONAL, INC.
CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS
(unaudited)
                                 
    Three Months Ended June 30,     Six Months Ended June 30,  
    2011     2010     2011     2010  
 
                               
Net loss
  $ (10,096,028 )   $ (9,982,049 )   $ (19,527,046 )   $ (14,526,364 )
Foreign currency translation adjustments
    64,938       (139,455 )     91,445       (62,738 )
Unrealized gain (loss) on investments
    7,751       (21,332 )     (25,307 )     (45,124 )
 
                       
Comprehensive loss
  $ (10,023,339 )   $ (10,142,836 )   $ (19,460,908 )   $ (14,634,226 )
 
                       
The accompanying notes are an integral part of these financial statements.

 

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HEARTWARE INTERNATIONAL, INC.
CONDENSED CONSOLIDATED STATEMENT OF STOCKHOLDERS’ EQUITY
(unaudited)
                                                 
                                    Accumulated        
    Common Shares     Additional             Other        
    Shares             Paid-In     Accumulated     Comprehensive        
    Issued     Amount     Capital     Deficit     Loss     Total  
 
Balance, December 31, 2010
    13,878,686     $ 13,879     $ 302,533,344     $ (127,268,545 )   $ (7,514,324 )   $ 167,764,354  
Issuance of common stock pursuant to share-based awards
    47,298       47       599,567                   599,614  
Share-based compensation
                6,436,813                   6,436,813  
Net loss
                      (19,527,046 )           (19,527,046 )
Other comprehensive loss:
                                               
Foreign currency translation adjustment
                            91,445       91,445  
Unrealized loss on investments
                            (25,307 )     (25,307 )
 
                                   
Balance, June 30, 2011
    13,925,984     $ 13,926     $ 309,569,724     $ (146,795,591 )   $ (7,448,186 )   $ 155,339,873  
 
                                   
The accompanying notes are an integral part of these financial statements.

 

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HEARTWARE INTERNATIONAL, INC.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(unaudited)
                 
    Six Months Ended June 30,  
    2011     2010  
 
CASH FLOWS FROM OPERATING ACTIVITIES
               
Net loss
  $ (19,527,046 )   $ (14,526,364 )
 
Adjustments to reconcile net loss to net cash used in operating activities:
               
Depreciation of property, plant and equipment
    1,019,609       580,536  
Amortization of intangible assets
    63,887       47,862  
Share-based compensation expense
    6,436,813       5,998,962  
Amortization of premium on investments
    440,507       167,056  
Amortization of discount on convertible senior notes
    2,597,153        
Amortization of deferred financing costs
    139,252        
Other
    340,100       284,998  
Change in operating assets and liabilities:
               
Accounts receivable
    3,526,642       3,528,615  
Inventories, net
    (7,547,061 )     (6,757,485 )
Prepaid expenses and other current assets
    (2,247,717 )     (389,974 )
Accounts payable
    (554,869 )     356,854  
Accrued expenses and other current liabilities
    1,309,423       1,430,473  
 
           
Net cash used in operating activities
    (14,003,307 )     (9,278,467 )
 
               
CASH FLOWS FROM INVESTING ACTIVITIES
               
Purchases of investments
    (80,128,177 )     (16,644,600 )
Maturities of investments
    25,000,000        
Additions to property, plant and equipment
    (4,667,787 )     (2,497,481 )
Additions to patents
    (253,940 )     (283,410 )
Proceeds from disposition of assets
    98,225        
 
           
Net cash used in investing activities
    (59,951,679 )     (19,425,491 )
 
               
CASH FLOWS FROM FINANCING ACTIVITIES
               
Proceeds from issuance of common stock
          62,760,450  
Payment of common stock issuance costs
    (600 )     (4,359,934 )
Proceeds from exercise of stock options
    599,614       2,804,101  
 
           
Net cash provided by financing activities
    599,014       61,204,617  
 
               
Effect of exchange rate changes on cash and cash equivalents
    51,334       (9,402 )
 
           
(DECREASE) INCREASE IN CASH AND CASH EQUIVALENTS
    (73,304,638 )     32,491,257  
 
               
CASH AND CASH EQUIVALENTS — BEGINNING OF PERIOD
    192,148,312       50,834,714  
 
           
 
               
CASH AND CASH EQUIVALENTS — END OF PERIOD
  $ 118,843,674     $ 83,325,971  
 
           
The accompanying notes are an integral part of these financial statements.

 

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HEARTWARE INTERNATIONAL, INC.
NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)
Note 1. Basis of Presentation
HeartWare International, Inc., referred to in these notes collectively with its subsidiaries HeartWare Pty. Limited, HeartWare, Inc., HeartWare (UK) Limited and HeartWare GmbH as “we,” “our,” “HeartWare” or the “Company,” is a medical device company that develops and manufactures small implantable heart pumps, or ventricular assist devices, used in the treatment of advanced heart failure.
The accompanying unaudited interim condensed consolidated financial statements have been prepared pursuant to the rules and regulations of the Securities and Exchange Commission (“SEC”) for reporting of interim financial information. Pursuant to such rules and regulations, certain information and footnote disclosures normally included in financial statements prepared in accordance with accounting principles generally accepted in the United States have been condensed or omitted. Accordingly, these statements do not include all the disclosures normally required by accounting principles generally accepted in the United States for annual financial statements and should be read in conjunction with Management’s Discussion and Analysis of Financial Condition and Results of Operations contained in this report and the audited financial statements and notes thereto for the year ended December 31, 2010 included in our Annual Report on Form 10-K. The accompanying condensed consolidated balance sheet as of December 31, 2010 has been derived from our audited financial statements. The condensed consolidated statements of operations for the three and six months ended June 30, 2011 and cash flows for the six months ended June 30, 2011 are not necessarily indicative of the results to be expected for any future period or for the year ending December 31, 2011.
In the opinion of management, the accompanying unaudited interim condensed consolidated financial statements contain all adjustments (consisting of only normally recurring adjustments) necessary to present fairly the financial position and results of operations as of the dates and for the periods presented.
Note 2. Liquidity
At June 30, 2011, we had approximately $198.8 million of cash, cash equivalents and investments. The accompanying condensed consolidated financial statements have been prepared in conformity with accounting principles generally accepted in the United States, which contemplates continuation of the Company as a going concern. We have sustained substantial losses from operations since our inception, and such losses have continued through June 30, 2011. At June 30, 2011, we had an accumulated deficit of approximately $146.8 million.
We have financed our operations primarily through the issuance of shares of our common stock and the issuance of convertible notes. Most recently, in December 2010, we consummated the issuance and sale of $143.75 million aggregate principal amount of convertible notes. The convertible notes are the senior unsecured obligations of the Company. The convertible notes bear interest at a rate of 3.5% per annum, payable semi-annually in arrears on June 15 and December 15 of each year, beginning on June 15, 2011. The convertible notes will mature on December 15, 2017, unless earlier repurchased or converted. The convertible notes will be convertible at an initial conversion rate of 10 shares of common stock per $1,000 principal amount of convertible notes, which corresponds to an initial conversion price of $100.00 per share of common stock.
For the remainder of 2011, our cash, cash equivalents and investments are expected to primarily be used to fund our ongoing operations including expanding our sales and marketing capabilities on a global basis, continuing our ENDURANCE trial for destination therapy, enrolling additional patients in our ADVANCE trial under a Continued Access Protocol (“CAP”), continued product development, regulatory and other compliance functions, including costs related to testing and submission of our PMA application, as well as for general working capital. We believe our cash, cash equivalent and investment balances are sufficient to support our planned operations through 2012.

 

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Note 3. Significant Accounting Policies
Principles of Consolidation
The condensed consolidated financial statements include the accounts of HeartWare International, Inc., and its subsidiaries described in Note 1. All inter-company balances and transactions have been eliminated in consolidation.
Accounting Estimates
The preparation of consolidated financial statements in conformity with accounting principles generally accepted in the United States (“US GAAP”) requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities, the disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting periods. Actual results could differ from those estimates.
Cash and Cash Equivalents
Cash and cash equivalents are recorded in the condensed consolidated balance sheets at cost, which approximates fair value. All highly liquid investments with an original maturity of three months or less at the date of purchase are considered to be cash equivalents.
Investments
Our investments classified as available-for-sale are stated at fair value with unrealized gains and losses reported in accumulated other comprehensive loss within stockholders’ equity. We classify our available-for-sale investments as short-term if their remaining time to maturity at purchase is beyond three months. Investments with maturities beyond one year may be classified as short-term based on their highly liquid nature and because such marketable securities represent the investment of cash that is available for current operations. Interest on investments classified as available-for-sale is included in investment income, net. Premiums paid on our short-term investments are amortized over the remaining term of the investment and such amortization is included in investment income, net.
Receivables
Accounts receivable consists of amounts due from the sale of our HeartWare® Ventricular Assist System (the “HeartWare System”) to our customers, which include hospitals, health research institutions and medical device distributors. Our receivables are geographically dispersed, with a significant portion from customers located in Europe and other foreign countries. As of June 30, 2011 and December 31, 2010, one customer had an accounts receivable balance representing approximately 11% and 13%, respectively, of our total accounts receivable.
We maintain allowances for doubtful accounts for estimated losses that may result from an inability to collect payments owed to us for product sales. We regularly review the allowance by considering factors such as historical experience, the age of the accounts receivable balances and current economic conditions that may affect a customer’s ability to pay.

 

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The following table summarizes the change in our allowance for doubtful accounts for the six months ended June 30, 2011 and 2010:
                 
    Six months ended  
    June 30,  
    2011     2010  
Beginning balance
  $ 600,000     $  
Additions (bad debt expense)
    300,000       285,000  
Deductions (charge-offs)
           
 
           
Ending balance
  $ 900,000     $ 285,000  
 
           
As of June 30, 2011 and December 31, 2010, we did not have an allowance for returns.
Inventories, net
Inventories are stated at the lower of cost or market. Cost is determined using a first-in, first-out, or FIFO, method. Work-in-process and finished goods include direct and indirect labor and manufacturing overhead. Finished goods include product which is ready-for-use and which is held by us or by our customers on a consignment basis.
We review our inventory for excess or obsolete inventory and write-down obsolete or otherwise unmarketable inventory to its estimated net realizable value. Obsolescence may occur due to product expiring or product improvements rendering previous versions obsolete. In May 2011, we began shipping a sintered version of the HeartWare System on a global basis. Sintering is commonly used in medical devices to facilitate tissue adhesion. The extent to which this product enhancement will cause obsolescence of existing non-sintered inventory is difficult to determine because the rate of product adoption of sintered product is dependent on individual customer acceptance, implantation rates and approval timeframes of Institutional Review Boards at U.S. sites. As of June 30, 2011, we had $3.5 million of non-sintered inventory on hand and this product continues to be implanted at customer sites. However, a write-down of all or a portion of this inventory as obsolete could have a material impact on our results of operations.
Deferred Financing Costs
Costs incurred in connection with the issuance of our convertible senior notes in December 2010 have been allocated between the liability component and the equity component as further discussed in Note 11. The liability component of the issuance costs incurred was capitalized and is included in deferred financing costs, net on the condensed consolidated balance sheets. These costs are being amortized using the effective interest method through December 15, 2017, the maturity date of the notes, and such amortization expense is reflected in interest expense on our condensed consolidated statements of operations. The amount of amortization for the three and six months ended June 30, 2011 was approximately $71,000 and $139,000, respectively.
Product Warranty
Certain patient accessories sold with the HeartWare System are covered by a limited warranty ranging from one to two years. Estimated contractual warranty obligations are recorded as an expense when the related revenue is recognized and are included in cost of revenues on the condensed consolidated statements of operations. Factors that affect the estimated warranty liability include the number of units sold, historical and anticipated rates of warranty claims, cost per claim, and vendor supported warranty programs. We periodically assess the adequacy of our recorded warranty liabilities and adjust the amounts as necessary.
The amount of the liability recorded is equal to the estimated costs to repair or otherwise satisfy claims made by customers. Accrued warranty expense is included as a component of accrued expenses and other current liabilities on the condensed consolidated balance sheets.

 

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The costs to repair or replace products associated with product recalls and voluntary service campaigns are recorded when they are determined to be probable and reasonably estimable as a cost of revenues and are not included in the product warranty liability. No such costs were incurred in the six months ended June 30, 2011 and approximately $411,000 was incurred in the six months ended June 30, 2010.
The following table summarizes the change in our warranty liability for the six months ended June 30, 2011 and 2010:
                 
    Six months ended  
    June 30,  
    2011     2010  
Beginning balance
  $ 290,891     $ 99,169  
Accrual for (reversal of) warranty expense
    (20,491 )     97,362  
Warranty costs incurred during the period
    (28,295 )     (47,363 )
 
           
Ending balance
  $ 242,105     $ 149,168  
 
           
Fair Value Measurements
The carrying amounts reported in the condensed consolidated balance sheets for cash and cash equivalents, accounts receivable, accounts payable and accrued expenses and other current liabilities approximate their fair value based on the short-term maturity of these instruments. Investments are considered available-for-sale as of June 30, 2011 and December 31, 2010 and are carried at fair value. See Note 6, “Fair Value Measurements” and Note 10, “Debt” for more information.
Vendor Concentration
For the three and six months ended June 30, 2011, we purchased approximately 55% of our inventory components and supplies from two vendors. For the three and six months ended June 30, 2010, we purchased approximately 62% and 51%, respectively, of our inventory components and supplies from the same two vendors. In addition, one of these vendors supplies consulting services and material used in research and development activities. As of June 30, 2011 and 2010, the amounts due to these vendors totaled approximately $788,000 and $1.1 million, respectively.
Concentration of Credit Risk and other Risks and Uncertainties
Financial instruments that potentially expose us to concentrations of credit risk consist primarily of cash and cash equivalents, investments and trade accounts receivable. Cash and cash equivalents are primarily on deposit with financial institutions in the United States and these deposits generally exceed the amount of insurance provided by the Federal Deposit Insurance Corporation (the “FDIC”). The Company has not experienced any historical losses on its deposits of cash and cash equivalents. Our investments consist of investment grade rated corporate and government agency debt.
Concentration of credit risk with respect to our trade accounts receivable from our customers is primarily limited to hospitals, health research institutions and medical device distributors. Credit is extended to our customers, based on an evaluation of a customer’s financial condition and collateral is not required. To date, we have not experienced any credit losses, but have established an allowance for doubtful accounts of $900,000 at June 30, 2011.
We are subject to certain risks and uncertainties including, but not limited to, our ability to achieve profitability, to generate cash flow sufficient to satisfy our indebtedness, to run clinical trials in order to receive and maintain FDA and foreign regulatory approvals for our products, the ability to achieve widespread acceptance of our product, our ability to manufacture our products in a sufficient volume and at a reasonable cost, the ability to protect our proprietary technologies and develop new products, the risks associated with operating in foreign countries, and general competitive and economic conditions. Changes in any of the preceding areas could have a material adverse effect on our business, results of operations or financial position.

 

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New Accounting Standards
In May 2011, the Financial Accounting Standards Board (FASB) issued Accounting Standards Update (ASU) No. 2011-04, Fair Value Measurement (Topic 820): Amendments to Achieve Common Fair Value Measurement and Disclosure Requirements in U.S. GAAP and IFRSs. ASU No. 2011-04 clarifies some existing concepts, eliminates wording differences between U.S. GAAP and International Financial Reporting Standards (“IFRS”), and in some limited cases, changes some principles to achieve convergence between U.S. GAAP and IFRS. ASU No. 2011-04 results in a consistent definition of fair value and common requirements for measurement of and disclosure about fair value between U.S. GAAP and IFRS. ASU No. 2011-04 also expands the disclosures for fair value measurements that are estimated using significant unobservable (Level 3) inputs. The provisions of ASU No. 2011-04 will become effective for us on January 1, 2012 and are to be applied prospectively. We do not expect the adoption of the provisions of ASU No. 2011-04 to have a material effect on our consolidated financial position, results of operations or cash flows and we do not expect to materially modify or expand our financial statement footnote disclosures.
In June 2011, the FASB issued ASU No. 2011-05, Comprehensive Income (Topic 220): Presentation of Comprehensive Income. ASU No. 2011-05 requires an entity to present the total of comprehensive income, the components of net income, and the components of other comprehensive income either in a single continuous statement of comprehensive income, or in two separate but consecutive statements. ASU No. 2011-05 eliminates the option to present components of other comprehensive income as part of the statement of stockholders’ equity. The presentation requirements will become effective for us on January 1, 2012. As ASU No. 2011-05 applies to financial statement presentation matters, the adoption of ASU No. 2011-05 will not affect our consolidated financial position, results of operations or cash flows and we believe our current presentation of comprehensive income complies with the new presentation requirements.
Note 4. Investments
We have cash investment policies that limit investments to investment grade securities. At June 30, 2011 and December 31, 2010, all of our investments were classified as available-for-sale and carried at fair value. Our investments in corporate debt are guaranteed by the FDIC or foreign governments. At June 30, 2011, all of our investments had maturity dates of less than twenty-four months.
The amortized cost and fair value of our investments, with gross unrealized gains and losses, were as follows:
At June 30, 2011
                                 
            Gross     Gross        
    Amortized     Unrealized     Unrealized     Aggregate  
    Cost Basis     Gains     Losses     Fair Value  
 
Short-term investments:
                               
U.S. government agency debt
  $ 49,806,325     $ 6,982     $ (22,236 )   $ 49,791,071  
Corporate debt
    15,182,732       24,329             15,207,061  
Certificates of deposit
    15,000,000                   15,000,000  
 
                       
 
                               
Total short-term investments
  $ 79,989,057     $ 31,311     $ (22,236 )   $ 79,998,132  
 
                       

 

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     At December 31, 2010
                                 
            Gross     Gross        
    Amortized     Unrealized     Unrealized     Aggregate  
    Cost Basis     Gains     Losses     Fair Value  
 
Short-term investments:
                               
Corporate debt
  $ 21,294,673     $ 35,437     $     $ 21,330,110  
 
                       
 
                               
Total short-term investments
  $ 21,294,673     $ 35,437     $     $ 21,330,110  
 
                       
 
                               
Long-term investments:
                               
U.S. government agency debt
  $ 4,006,714     $     $ (1,055 )   $ 4,005,659  
 
                       
 
                               
Total long-term investments
  $ 4,006,714     $     $ (1,055 )   $ 4,005,659  
 
                       
For the three and six months ended June 30, 2011 and 2010 we did not have any realized gains or losses on our investments.
Note 5. Foreign Exchange Instruments
During the quarter ended June 30, 2011, we entered into a foreign currency forward-exchange contract in an effort to minimize the risk of future fluctuations in the exchange rates between Australian dollars and Japanese Yen. The foreign currency forward-exchange contract was directly related to an asset purchase commitment by our Australian subsidiary. We do not utilize derivative financial instruments for speculative or trading purposes.
As of June 30, 2011, the forward contract to sell Australian dollars to Japanese Yen had a notional value of AU$858,000 and an exchange rate of one Australian dollar to 83.35 Japanese Yen. During the quarter ended June 30, 2011, the realized fair value of this forward exchange contract resulted in an expense of $16,000, which is included in other, net on the condensed consolidated statements of operations.
Note 6. Fair Value Measurements
FASB ASC 820 — Fair Value Measurements and Disclosures, defines fair value as the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement date. FASB ASC 820 requires disclosures about the fair value of all financial instruments, whether or not recognized, for financial statement purposes. Disclosures about the fair value of financial instruments are based on pertinent information available to us as of the reporting dates. Accordingly, the estimates presented in these condensed consolidated financial statements are not necessarily indicative of the amounts that could be realized on disposition of the financial instruments.
FASB ASC 820 specifies a hierarchy of valuation techniques based on whether the inputs to those valuation techniques are observable or unobservable. Observable inputs reflect market data obtained from independent sources, while unobservable inputs reflect market assumptions. The hierarchy gives the highest priority to unadjusted quoted prices in active markets for identical assets or liabilities (Level 1 measurement) and the lowest priority to unobservable inputs (Level 3 measurement).
The three levels of the fair value hierarchy are as follows:
Level 1 — Quoted prices for identical instruments in active markets.
Level 2 — Quoted prices for similar instruments in active markets; quoted prices for identical or similar instruments in markets that are not active; and model-derived valuations whose inputs are observable or whose significant value drivers are observable.
Level 3 — Instruments with primarily unobservable value drivers.

 

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The following table represents the fair value of our financial assets and financial liabilities measured at fair value on a recurring basis and which level was used in the fair value hierarchy.
                                         
    At June 30, 2011  
    Carrying     Fair     Fair Value Measurements at the Reporting Date Using  
    Value     Value     Level 1     Level 2     Level 3  
Assets
                                       
Short-term investments
  $ 79,998,132     $ 79,998,132     $     $ 79,998,132     $  
 
                                       
Liabilities
                                       
Foreign exchange instrument
    15,547       15,547             15,547        
Convertible senior notes
    91,518,710 (1)     151,117,188             151,117,188        
                                         
    At December 31, 2010  
    Carrying     Fair     Fair Value Measurements at the Reporting Date Using  
    Value     Value     Level 1     Level 2     Level 3  
Assets
                                       
Short-term investments
  $ 21,330,110     $ 21,330,110     $       21,330,110     $  
Long-term investments
    4,005,659       4,005,659             4,005,659        
 
                                       
Liabilities
                                       
Convertible senior notes
    88,921,557 (1)     160,693,813             160,693,813        
(1)   The carrying amount of our convertible senior notes is net of unamortized discount. See Note 11, “Debt” for more information.
The fair value of our investments was determined using quoted prices for the instruments in markets that are not active. The fair value of our foreign exchange instrument was determined using observable market data such as pricing for similar instruments or recently executed transactions. The fair value of our convertible senior notes was determined using observable market data (including trade data) and is presented for disclosure purposes only.
Note 7. Inventories, Net
Components of inventories, net are as follows:
                 
    June 30,     December 31,  
    2011     2010  
 
Raw material
  $ 5,194,259     $ 4,279,170  
Work-in-process
    4,181,495       2,708,840  
Finished goods
    13,146,602       8,088,580  
 
           
 
  $ 22,522,356     $ 15,076,590  
 
           
Finished goods inventories includes inventory held on consignment at customer sites of $5.4 million and $4.7 million, at June 30, 2011 and December 31, 2010, respectively.

 

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Note 8. Property, Plant and Equipment, Net
Property, plant and equipment, net consists of the following:
                         
    Estimated     June 30,     December 31,  
    Useful Lives     2011     2010  
Machinery and equipment
    1.5 to 7 years     $ 11,225,797     $ 8,966,747  
Leasehold improvements
    3 to 7 years       1,835,365       282,483  
Office equipment, furniture and fixtures
    5 to 7 years       913,516       450,849  
Purchased software
    5 to 7 years       2,104,057       1,741,132  
 
                   
 
            16,078,735       11,441,211  
Less: accumulated depreciation
            (4,948,383 )     (3,957,189 )
 
                   
 
          $ 11,130,352     $ 7,484,022  
 
                   
Note 9. Other Intangible Assets, Net
The gross carrying amount of intangible assets and the related accumulated amortization for intangible assets subject to amortization are as follows:
                                         
            June 30, 2011     December 31, 2010  
    Weighted Average Life     Gross Carrying     Accumulated     Gross Carrying     Accumulated  
Amortizable Intangible Assets   (Years)     Amount     Amortization     Amount     Amortization  
Patents
    15     $ 2,115,624     $ (330,115 )   $ 1,861,684     $ (266,228 )
Amortization expense for the three months ended June 30, 2011 and 2010 was approximately $33,000 and $25,000, respectively. Amortization expense for the six months ended June 30, 2011 and 2010 was approximately $64,000 and $48,000, respectively.
Note 10. Accrued Expenses and Other Current Liabilities
Accrued expenses and other current liabilities consist of the following:
                 
    June 30,     December 31,  
    2011     2010  
Accrued payroll and other employee costs
  $ 3,345,268     $ 4,152,833  
Accrued material purchases
    2,245,440       255,679  
Accrued professional fees
    693,538       577,237  
Accrued research and development costs
    436,839       671,928  
Accrued VAT
    356,690       647,525  
Accrued interest payable on convertible senior notes
    209,635       209,635  
Other accrued expenses
    1,043,679       486,513  
 
           
 
  $ 8,331,089     $ 7,001,350  
 
           
Accrued payroll and other employee costs included estimated year-end employee bonuses of approximately $1.9 million and $3.1 million at June 30, 2011 and December 31, 2010, respectively.
Note 11. Debt
Convertible Senior Notes
On December 15, 2010, we completed the sale of 3.5% convertible senior notes due 2017 (the “Convertible Notes”) for an aggregate principal amount of $143.75 million pursuant to the terms of an Indenture dated December 15, 2010. The Convertible Notes are the senior unsecured obligations of the Company. The Convertible Notes bear interest at a rate of 3.5% per annum, payable semi-annually in arrears on June 15 and December 15 of each year, beginning on June 15, 2011. The Convertible Notes will mature on December 15, 2017, unless earlier repurchased by us or converted.

 

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The Convertible Notes will be convertible at an initial conversion rate of 10 shares of our common stock per $1,000 principal amount of Convertible Notes, which corresponds to an initial conversion price of $100.00 per share of our common stock representing a conversion premium of approximately 23% based on the closing price of $81.31 per share of our common stock on December 9, 2010, the day the notes were priced. The conversion rate is subject to adjustment from time to time upon the occurrence of certain events.
Prior to June 15, 2017, holders may convert their Convertible Notes at their option only upon satisfaction of one or more conditions relating to the sale price of our common stock, the trading price per $1,000 principal amount of Convertible Notes or specified corporate events. On or after June 15, 2017, until the close of business of the business day immediately preceding the date the Convertible Notes mature, holders may convert their Convertible Notes at any time, regardless of whether any of the foregoing conditions have been met. As of the date of this report, none of the events that would allow holders to convert their Convertible Notes have occurred. Upon conversion, we will pay or deliver, as the case may be, cash, shares of our common stock or a combination thereof, at our election.
In accordance with ASC 470-20, Debt, which applies to certain convertible debt instruments that may be settled in cash or other assets, or partially in cash, upon conversion, we recorded the long-term debt and equity components on our Convertible Notes separately on the issuance date. The amount recorded for long-term debt was determined by measuring the fair value of a similar liability that does not have an associated equity component. The measurement of fair value required the Company to make estimates and assumptions to determine the present value of the cash flows of the Convertible Notes, absent the conversion feature. This treatment increased interest expense associated with our Convertible Notes by adding a non-cash component to amortize a debt discount calculated based on the difference between the 3.5% cash coupon rate and the effective interest rate on debt borrowing of approximately 12.5%. The discount is being amortized to interest expense through the December 15, 2017 maturity date of the Convertible Notes using the effective interest method and is included in interest expense on the condensed consolidated statements of operations. Additionally, we allocated the costs related to issuance of the Convertible Notes on the same percentage as the long-term debt and equity components, such that a portion of the costs is allocated to the long-term debt component and the equity component included in additional paid-in capital. The portion of the costs allocated to the long-term debt component is presented as deferred financing costs, net on our condensed consolidated balance sheets. These deferred financing costs are also being amortized to interest expense through the December 15, 2017 maturity date of the Convertible Notes using the effective interest method and such amortization is included in interest expense on the condensed consolidated statements of operations
The Convertible Notes and the equity component, which is recorded in additional paid-in-capital, consisted of the following:
                 
    June 30,     December 31,  
    2011     2010  
Principal amount
  $ 143,750,000     $ 143,750,000  
Unamortized discount
    (52,231,290 )     (54,828,443 )
 
           
Net carrying amount
  $ 91,518,710     $ 88,921,557  
 
           
Equity component
  $ 55,037,913     $ 55,037,913  
 
           
Based on the initial conversion rate of 10 shares of our common stock per $1,000 principal amount of Convertible Notes, which corresponds to an initial conversion price of $100.00 per share of our common stock, the number of shares issuable upon conversion of the Convertible Notes is 1,437,500. The value of these shares, based on the closing price of our common stock on June 30, 2011 of $74.08, was approximately $106.5 million. The fair value of our Convertible Notes as presented in Note 6 was $151.1 million and $160.7 million at June 30, 2011 and December 31, 2010, respectively.

 

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Interest expense related to the Convertible Notes consisted of interest due on the principal amount, amortization of the discount and amortization of the portion of the deferred financing costs allocated to the long-term debt component. For the three and six months ended June 30, 2011, interest expense related to the Convertible Notes was as follows:
                 
    Three Months     Six Months  
    Ended     Ended  
    June 30, 2011     June 30, 2011  
Stated amount at 3.5% coupon rate
  $ 1,257,812     $ 2,515,625  
Amortization of discount
    1,318,074       2,597,153  
Amortization of deferred financing costs
    70,672       139,252  
 
           
 
  $ 2,646,558     $ 5,252,030  
 
           
Note 12. Stockholders’ Equity
In February 2010, we completed a public offering of approximately 1.77 million shares of our common stock, including the underwriter’s exercise of their overallotment to purchase 230,595 shares, at an offering price of $35.50 per share for aggregate gross proceeds of approximately $62.8 million. The underwriters for the transaction received a fee of 6% of the gross proceeds. After fees and related expenses, net proceeds from the offering were approximately $58.5 million.
The offering was completed pursuant to a prospectus supplement, dated January 27, 2010, to a shelf registration statement on Form S-3 that was previously filed with the SEC and which was declared effective on January 20, 2010. This shelf registration statement allows us to offer and sell from time to time, in one or more series or issuances and on terms that we will determine at the time of the offering, any combination of the securities described in the prospectus, up to an aggregate amount of $100 million.
In the six months ended June 30, 2011, we issued an aggregate of 17,606 shares of our common stock upon the exercise of stock options and an aggregate of 29,692 shares of our common stock upon the vesting of restricted stock units.
Note 13. Share-Based Compensation
We recognize share-based compensation expense for the portion of awards that are ultimately expected to vest using an accelerated accrual method over the vesting period from the date of grant. We estimate forfeitures at the time of grant. We have applied a forfeiture rate of approximately 12.5% to all unvested share-based awards as of June 30, 2011, which represents the portion that we expect will be forfeited over the vesting period. We reevaluate this estimated rate periodically and adjust the forfeiture rate as necessary. Vesting of share-based awards issued with performance-based vesting criteria must be “probable” before we begin recording share-based compensation expense. At each reporting period, we review the likelihood that these awards will vest and if the vesting is deemed probable, we begin to recognize compensation expense at that time. If ultimately performance goals are not met, for any awards where vesting was previously deemed probable, previously recognized compensation cost will be reversed.

 

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We allocate share-based compensation expense to cost of revenues, selling, general and administrative expense and research and development expense based on the award holders’ employment function. For the three and six months ended June 30, 2011 and 2010, we recorded share-based compensation expense as follows:
                                 
    Three Months Ended     Six Months Ended  
    June 30,     June 30,  
    2011     2010     2011     2010  
Cost of revenues
  $ 533,644     $ 207,270     $ 1,118,862     $ 475,920  
Selling, general and administrative
    2,209,086       3,577,919       3,653,435       4,479,977  
Research and development
    758,703       487,306       1,664,516       1,043,065  
 
                       
 
  $ 3,501,433     $ 4,272,495     $ 6,436,813     $ 5,998,962  
 
                       
No deferred tax benefits were attributed to our share-based compensation expense recorded in the accompanying condensed consolidated financial statements because we are in a net operating loss position and a full valuation allowance is maintained for all net deferred tax assets. We receive a tax deduction for certain stock option exercises during the period the options are exercised, and for the vesting of restricted stock units during the period the restricted stock units vest. For stock options, the amount of the tax deduction is generally for the excess of the fair market value of our shares of common stock over the exercise price of the stock options at the date of exercise. For restricted stock units, the amount of the tax deduction is generally for the fair market value of our shares of common stock at the vesting date. Excess tax benefits are not included in the accompanying condensed consolidated financial statements because we are in a net operating loss position and a full valuation allowance is maintained for all net deferred tax assets.
Equity Plans
We have issued share-based awards to employees, non-executive directors and outside consultants through various approved plans and outside of any formal plan. New shares are issued upon the exercise of share-based awards.
On August 5, 2008, we adopted the HeartWare International, Inc. 2008 Stock Incentive Plan (“2008 SIP”). The 2008 SIP allows for the issuance of share-based awards to employees, directors and consultants. We have issued options and restricted stock units (“RSU’s”) to employees and directors under the 2008 SIP. The plan allows for the issuance of share-based awards representing up to 13% of the prior fiscal year’s weighted average shares outstanding, less share-based awards outstanding under our other equity plans. At June 30, 2011, there were approximately 619,000 shares available for future awards under the 2008 SIP.
Stock Options
Each option allows the holder to subscribe for and be issued one share of our common stock at a specified price, which is generally the quoted market price of our common stock on the date the option is issued. Options generally vest on a pro-rata basis on each anniversary of the issuance date within four years of the date the option is issued. Options may be exercised after they have vested and prior to the specified expiry date provided applicable exercise conditions are met, if any. The expiry date can be for periods of up to ten years from the date the option is issued.
In 2007 and 2008, we granted options with performance-based vesting criteria. These performance-based options vest in four equal tranches contingent upon the achievement of pre-determined corporate milestones related primarily to the development of our products and the achievement of certain prescribed clinical and regulatory objectives. Any performance-based options that have not vested after five years from the date of grant automatically expire.

 

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The fair value of each option is estimated on the date of grant using the Black-Scholes option pricing model using the assumptions established at that time. The following table includes the assumptions used for options issued in the three and six months ended June 30, 2011 and 2010.
                                 
    Three Months Ended     Six Months Ended  
    June 30,     June 30,  
    2011     2010     2011     2010  
Dividend yield
    0 %     0 %     0 %     0 %
Expected volatility
    58.24 %     60.53 %     58.31 %     61.05 %
Risk-free interest rate
    2.10 %     2.63 %     2.16 %     2.81 %
Estimated holding period (years)
    6.25       6.25       6.25       6.25  
Information related to options granted under all of our plans at June 30, 2011 and activity in the six months then ended is as follows (certain amounts in US$ were converted from AU$ at the then period-end spot rate):
                                 
                    Weighted        
            Weighted     Average        
            Average     Remaining        
            Exercise     Contractual Life     Aggregate  
    Shares     Price     (Years)     Intrinsic Value  
Outstanding at December 31, 2010
    404,366     $ 32.87                  
Granted
    13,750       78.47                  
Exercised
    (17,606 )     34.06                  
Forfeited
    (8,991 )     37.51                  
Expired
                           
 
                             
Outstanding at June 30, 2011
    391,519     $ 35.37       6.31     $ 15,154,284  
 
                             
Exercisable at June 30, 2011
    246,960     $ 36.10       5.49     $ 9,379,109  
 
                             
The aggregate intrinsic values at June 30, 2011 noted in the table above represent the closing price of our common stock traded on NASDAQ, less the weighted average exercise price at period end multiplied by the number of options outstanding or exercisable.
At June 30, 2011, 34,283 of the 144,559 options outstanding that are not yet exercisable are subject to performance-based vesting criteria as described above.
The weighted average grant date fair value per share of options issued in the six months ended June 30, 2011 and 2010 was $44.36 and $27.08 per share, respectively.
The total intrinsic value of options exercised in the six months ended June 30, 2011 was approximately $971,000. Cash received from options exercised in the six months ended June 30, 2011 was approximately $600,000. The total intrinsic value of options exercised in the six months ended June 30, 2010 was approximately $2.8 million. Cash received from options exercised in the six months ended June 30, 2010 was approximately $2.8 million.
At June 30, 2011, there was approximately $1.4 million of unrecognized compensation cost related to non-vested option awards, including performance-based options not yet deemed probable of vesting. The expense is expected to be recognized over a weighted average period of 1.2 years.
Restricted Stock Units
RSU’s issued under the plans vest on a pro-rata basis on each anniversary of the issuance date over three or four years or vest in accordance with performance-based criteria. The RSU’s with performance-based vesting criteria vest in tranches contingent upon the achievement of pre-determined corporate milestones related primarily to the development of our products and the achievement of certain prescribed clinical and regulatory objectives. RSU’s with performance-based vesting criteria not vested after five years from the date of grant automatically expire. There is no consideration payable on the vesting or exercise of RSU’s issued under the plans. Upon vesting, the RSU’s are exercised automatically and settled in shares of our common stock.

 

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Information related to RSU’s at June 30, 2011 and activity in the six months then ended is as follows:
                         
            Weighted        
            Average        
            Remaining        
            Contractual        
    Number of     Life     Aggregate  
    Units     (Years)     Intrinsic Value  
Outstanding at December 31, 2010
    544,865                  
Granted
    65,450                  
Vested/Exercised
    (29,692 )                
Forfeited
    (18,905 )                
Expired
                     
 
                     
Outstanding at June 30, 2011
    561,718       1.42     $ 41,612,069  
 
                     
Exercisable at June 30, 2011
              $  
 
                     
The aggregate intrinsic value at June 30, 2011 noted in the table above represents the closing price of our common stock traded on NASDAQ, multiplied by the number of RSU’s outstanding.
At June 30, 2011, 56,257 of the 561,718 RSU’s outstanding that are not yet exercisable are subject to performance-based vesting criteria as described above.
The total intrinsic value of RSU’s vested in the six months ended June 30, 2011 and 2010 was approximately $2.5 million and $2.6 million, respectively.
The fair value of each RSU award equals the closing price of our common stock on the date of grant. The weighted average grant date fair value per share of RSU’s granted in the six months ended June 30, 2011 and 2010 was $78.77 and $55.33, respectively.
At June 30, 2011, we had approximately $16.6 million of unrecognized compensation cost related to non-vested RSU awards, including awards not yet deemed probable of vesting. The expense is expected to be recognized over a weighted average period of 1.3 years.
Note 14. Net Loss Per Common Share
Basic net loss per common share is computed by dividing net loss for the period by the weighted-average number of common shares outstanding during the period. Diluted net loss per common share adjusts basic net loss per common share for the dilutive effects of convertible securities, options and other potentially dilutive instruments only in the periods in which such effect is dilutive. Due to our net loss for all periods presented, all potentially dilutive instruments were excluded because their inclusion would have been anti-dilutive. The following instruments have been excluded from the calculation of diluted net loss per common share, as their effect would be anti-dilutive.
                 
    Three and Six Months Ended  
    June 30,  
    2011     2010  
Common shares issuable upon:
               
Conversion of convertible senior notes
    1,767,923        
Exercise of share-based awards
    953,237       915,201  
Note 15. Business Segment, Geographic Areas and Major Customers
For financial reporting purposes, we have one reportable segment which designs, manufactures and markets medical devices for the treatment of advanced heart failure. Generally, products are sold to customers located in the United States through our clinical trials, as commercial products to customers in Europe and under special access in other countries. Product sales attributed to a country or region are based on the location of the customer to whom the products are sold. Long-lived assets are primarily held in the United States.

 

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Product sales by geographic location are as follows:
                                 
    Three Months Ended     Six Months Ended  
    June 30,     June 30,  
(in thousands)   2011     2010     2011     2010  
Domestic
  $ 6,291     $ 1,865     $ 12,189     $ 4,547  
Germany
    8,214       5,283       13,712       10,839  
International, excluding Germany
    5,884       2,609       12,463       5,074  
 
                       
 
  $ 20,389     $ 9,757     $ 38,364     $ 20,460  
 
                       
For the three and six months ended June 30, 2011, one customer accounted for approximately 11% and 10%, respectively, of product sales in the aggregate. For the three and six months ended June 30, 2010, two customers exceeded 10% of product sales individually and accounted for approximately 30% and 29%, respectively, of product sales in the aggregate. As the majority of our revenue is generated outside of the U.S., we are dependent on favorable economic and regulatory environments for our products in Europe and other countries outside of the U.S.
The percentage of our revenue generated in the U.S. was lower in 2010 compared to 2011 due to the completion of enrollment in our ADVANCE trial in the U.S. in February 2010. While the FDA approved an Investigational Device Exemption Supplement that allowed us to enroll additional patients in our ADVANCE trial under a Continued Access Protocol, we did not recommence enrollment in our ADVANCE trial until the second quarter of 2010 while we awaited approval. Also contributing to the increase in the percentage of our revenue generated in the U.S. in 2011 was continued enrollment in our ENDURANCE destination therapy clinical trial in the U.S., which commenced in August 2010.
Note 16. Commitments and Contingencies
At June 30, 2011, we had purchase order commitments of approximately $26.3 million related to product costs and property, plant and equipment purchases. Many of our materials and supplies require long lead times and as such purchase order commitments reflect materials that may be received up to one year from the date of order.
From time to time we may be involved in litigation or other contingencies arising in the ordinary course of business. Except as set forth below or in our 2010 Annual Report on Form 10-K, and based on the information presently available, management believes that there are no contingencies, claims or actions, pending or threatened, the ultimate resolution of which will have a material adverse effect on our financial position, liquidity or result of operations.
On February 24, 2010 we received a letter from two holders of Series A Preferred Stock in HeartWare, Inc., an indirect subsidiary of HeartWare International, Inc. These holders requested various financial and other information regarding HeartWare, Inc. for the purpose of determining the Company’s compliance with their rights as holders of Series A Preferred Stock, including whether a liquidation event has occurred since inception in 2003. HeartWare, Inc. issued Series A-1 and Series A-2 Preferred Stock to certain equity holders of Kriton Medical, Inc. when HeartWare, Inc. purchased substantially all of the assets of Kriton in July 2003. The Series A-1 and Series A-2 Preferred Stock do not have voting or dividend rights but entitle the holders thereof to receive, upon certain liquidation events of HeartWare, Inc. (but not the liquidation of or change of control of HeartWare International, Inc.), an amount equal to $10 per share of Series A-1 and $21 per share of Series A-2. The aggregate liquidation preference payment obligation totals approximately $15 million.

 

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On June 27, 2011, HeartWare International, Inc. and HeartWare, Inc., along with HeartWare’s directors, certain officers and a significant stockholder, were named as defendants in a putative class action lawsuit filed in Massachusetts state court by two other Series A Preferred Stockholders on behalf of all holders of Series A Preferred Stock. The complaint alleges that the defendants breached their fiduciary and contractual obligations to Series A Preferred Stockholders by preventing them from receiving a payment of the liquidation preference in connection with certain corporate transactions, including a transaction in 2005 in which HeartWare, Inc. was acquired by HeartWare Limited, a subsidiary of HeartWare International, Inc. The plaintiffs seek monetary damages, interest, costs and limited equitable relief. We do not believe HeartWare International, Inc., HeartWare, Inc. or any of our directors, officers or stockholders have abrogated the rights, or in any way failed to satisfy obligations owed to, any of our stockholders, including holders of Series A Preferred Stock. We intend to vigorously defend the suit.
In accordance with ASC 450, Contingencies, we accrue loss contingencies including costs of settlement, damages and defense related to litigation to the extent they are probable and estimable. Otherwise, we expense these costs as incurred. If the estimate of a probable loss is a range and no amount within the range is more likely, we accrue the minimum amount of the range. As of June 30, 2011 we have not accrued any amounts related to the above litigation.
Note 17. Subsequent Events
We have evaluated events and transactions that occurred subsequent to June 30, 2011 through the date the financial statements were issued, for potential recognition or disclosure in the accompanying condensed consolidated financial statements.
We did not identify any events or transactions that should be recognized or disclosed in the accompanying condensed consolidated financial statements.

 

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ITEM 2:   MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
The following discussion and analysis of our financial condition and results of operations should be read together with our unaudited interim condensed consolidated financial statements and related notes appearing elsewhere in this Quarterly Report on Form 10-Q. Certain abbreviated key terms have the meanings defined elsewhere in this Quarterly Report on Form 10-Q.
Overview
HeartWare develops and manufactures small implantable heart pumps, or ventricular assist devices, for the treatment of advanced heart failure.
The HeartWare® Ventricular Assist System (the “HeartWare System”), which includes a left ventricular assist device (“LVAD”), or blood pump, patient accessories and surgical tools, is designed to provide circulatory support for patients in the advanced stage of heart failure. The core of the HeartWare System is a proprietary continuous flow blood pump, the HVAD Pump, which is a full-output device capable of pumping up to 10 liters of blood per minute. The HeartWare System is designed to be implanted adjacent to the heart, avoiding the abdominal surgery generally required to implant similar devices.
In 2009, we received CE Marking for the HeartWare System in the European Union allowing for commercial sale and distribution of our device. In the U.S., the device is the subject of clinical trials for two indications: bridge-to-transplant and destination therapy. Our device is also available in other countries around the world under special access programs.
Recent key milestones in the development and commercialization of the HeartWare System include the following:
    FDA approval of an Investigational Device Exemption (IDE) Supplement that allows us to enroll a third allotment, of 94 additional patients, in our ADVANCE bridge-to-transplant clinical trial under a Continued Access Protocol (CAP);
    Submission of a Pre-Market Approval application for our HeartWare System based on data generated in our ADVANCE bridge-to-transplant clinical trial and subsequent acceptance by the FDA of the application for filing and substantive review;
    Being named to the REVIVE-IT study, a study to be completed by the Universities of Michigan and Pittsburgh on the benefits of LVAD’s in patients with earlier access to the device;
    Approval of the HeartWare System by the Therapeutic Goods Administration (TGA) in Australia for listing on the Australian Register of Therapeutic Goods;
    Approval by the U.S. FDA for use in our clinical trials and notification of acceptance by the British Standards Institution of a sintered inflow tube; and
    Reimbursement approval in France and Belgium of the HeartWare System.
Beyond the HeartWare System, we are also evaluating our next generation device, the MVAD. The MVAD is based on the same technology platform as the HeartWare System but adopts an axial flow, rather than a centrifugal flow approach, and is being developed in multiple configurations. Several MVAD configurations are in preclinical development. The pericardial MVAD configuration is currently undergoing final Good Laboratory Practices (“GLP”) in-vivo testing in preparation for a 2012 clinical trial. We believe that the MVAD designs will be implantable by surgical techniques that are even less invasive than those required to implant the HVAD Pump.

 

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We began generating revenue from our products in August 2008 and have incurred net losses in each year since our inception. We expect our losses to continue as we advance and expand our clinical trial activities in the U.S., continue to develop commercial markets outside of the U.S., and expand our research and development into next generation products including the MVAD.
We have financed our operations primarily through the issuance of convertible notes and the issuance of shares of our common stock. Most recently, on December 15, 2010, we issued convertible notes with an aggregate principal amount of $143.75 million pursuant to the terms of an Indenture dated as of December 15, 2010. The convertible notes are senior unsecured obligations of the Company. The convertible notes bear interest at a rate of 3.5% per annum, payable semi-annually in arrears on June 15 and December 15 of each year, beginning on June 15, 2011. The convertible notes will mature on December 15, 2017, unless earlier repurchased or converted.
We are headquartered in Framingham, Massachusetts. We have an operations and manufacturing facility in Miami Lakes, Florida, a small development and operations facility in Sydney, Australia and a small distribution and customer service facility in Hannover, Germany.
Critical Accounting Policies and Estimates
We prepare our financial statements in accordance with accounting principles generally accepted in the United States. We are required to adopt various accounting policies and to make estimates and assumptions in preparing our financial statements that affect the reported amounts of our assets, liabilities, revenue and expenses. Our significant accounting policies are disclosed in Note 3 to the Consolidated Financial Statements included in our Annual Report on Form 10-K for the fiscal year ended December 31, 2010 (“2010 Annual Report on Form 10-K”) filed with the Securities and Exchange Commission on February 24, 2011. Our most critical accounting policies and estimates include: revenue recognition, inventory capitalization, accounting for share-based compensation, measurement of fair value, income taxes and reserves. We also have other key accounting policies that are less subjective and, therefore, their application would not have a material impact on our reported results of operations. On an ongoing basis, we evaluate our estimates and assumptions. We base our estimates on historical experience to the extent practicable and on various other assumptions that we believe are reasonable under the circumstances and at the time they are made. If our assumptions prove inaccurate or if our future results are not consistent with our historical experience, we may be required to make adjustments in our policies that affect our reported results. There have been no material changes to our critical accounting policies and estimates from the information provided in Part II, Item 7, Management’s Discussion and Analysis of Financial Condition and Results of Operations included in our 2010 Annual Report on Form 10-K.
Results of Operations
Three and six months ended June 30, 2011 and 2010
Revenues, net
In the three and six months ended June 30, 2011 and 2010, we generated revenue from commercial sales outside of the U.S. and sales in connection with our clinical trials in the U.S. The increase in revenue from the the comparable periods in 2010, is due to increased implants in the U.S., as we have two studies on-going as compared to one in 2010, and increased market penetration outside of the U.S.
                                                 
    Three Months Ended             Six Months Ended        
    June 30,             June 30,        
(in thousands)   2011     2010     Change     2011     2010     Change  
Revenues, net
  $ 20,389     $ 9,757       109 %   $ 38,364     $ 20,460       88 %

 

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For the three months ended June 30, 2011, approximately 69% of our product sales were derived from commercial sales outside of the United States, predominantly in Europe, compared to approximately 81% for the three months ended June 30, 2010.
For the six months ended June 30, 2011, approximately 68% of our product sales were derived from commercial sales outside of the United States, predominantly in Europe, compared to approximately 78% for the six months ended June 30, 2010.
We operate in multiple currencies outside of the US, with the majority of our international revenue denominated in Euro. During the three and six months ended June 30, 2011, our net international revenue increased $6.3 million, or 80%, and $10.3 million, or 65%, respectively, as compared to the same periods in the prior year. The change in exchange rates for all foreign currencies for the three and six months ended accounted for approximately $1.4 million of the increase in each period.
We expect to continue to generate and grow commercial revenue from product sales as we further expand our sales and marketing efforts outside of the United States, continue implanting in the U.S. under a CAP for our bridge-to-transplant clinical trial, and increase the number of implants in our destination therapy clinical trial, ENDURANCE, in the U.S. Notwithstanding our plans to generally expand our U.S. clinical programs, revenues from U.S. sources in connection with our trials may vary from quarter to quarter as the recruitment of qualified patients that meet protocol criteria fluctuate and additional CAP cohorts are subject to FDA approval.
Future product sales are dependent on many factors, including receiving and maintaining the necessary regulatory approvals in the U.S. and internationally, perception of product performance and market acceptance among physicians, patients, health care payers and the medical community as well as our capacity to meet customer demand by manufacturing sufficient quantities of our products.
Cost of Revenues
Cost of revenues includes costs associated with manufacturing our product and consists of direct materials, labor and overheard expenses allocated to the manufacturing process. Cost of revenues totaled approximately $7.9 million and $4.3 million in the three months ended June 30, 2011 and 2010, respectively. Cost of revenues totaled approximately $15.5 million and $10.0 million in the six months ended June 30, 2011 and 2010, respectively.
Gross profit and gross margin percentage are as follows:
                                 
    Three Months Ended     Six Months Ended  
    June 30,     June 30,  
(in thousands)   2011     2010     2011     2010  
Gross profit
  $ 12,476     $ 5,464     $ 22,855     $ 10,486  
Gross margin %
    61.2 %     56.0 %     59.6 %     51.3 %
Gross margin percentage for the three and six months ended June 30, 2011 increased compared to the same periods in 2010 as a result of lower per unit costs in 2011 primarily due to increased production volume and improved efficiencies in our manufacturing processes. In addition, gross margin for the six months ended June 30, 2010 was impacted by costs incurred in connection with the voluntary field corrective action we initiated in April 2010. The total cost of the repairs and replacements was approximately $411,000. The action was taken as a result of a limited number of reported issues related to the audio volume of alarm notifications and resulted in the repair or replacement of controllers in inventory, including controllers held on consignment at customer sites, and units previously distributed through clinical trials or sold to customers.
Selling, General and Administrative
Selling, general and administrative expenses include costs associated with selling and marketing our products and the general corporate administration of the Company. These costs are primarily related to salaries and wages and related employee costs, depreciation of fixed assets, travel, external consultants and contractors, legal and accounting fees and general infrastructure costs, and include all operating costs not associated with or otherwise classified as research and development costs or cost of revenues.
                                                 
    Three Months Ended June 30,     Six Months Ended June 30,  
(in thousands)   2011     2010     Change     2011     2010     Change  
Total selling, general and administrative
  $ 9,892     $ 7,688       29 %   $ 18,556     $ 12,245       52 %

 

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The increase of $2.2 million for the three months ended June 30, 2011 as compared to three months ended June 30, 2010 was primarily a result of an increase in employee costs, including salaries and wages and related costs, of approximately $1.4 million, primarily due to increased headcount to build our sales and marketing and administrative functions to support expected future growth. We also experienced increases in marketing expenses of $617,000, office expenses of $540,000, travel expenses of $482,000 and legal costs of $172,000. These increases were partially offset by a decrease in share-based compensation expense of approximately $1.4 million. The decrease in share-based compensation expense is due to the recognition of approximately $2.1 million of share-based compensation expense in the second quarter of 2010 related to a grant with a vesting period that would have begun in September 2009 but was subject to stockholder approval. Approval was obtained at our annual meeting of stockholders in the second quarter of 2010 resulting in a true-up of share-based compensation expense to coincide with the vesting period.
The increase of $6.3 million for the six months ended June 30, 2011 was primarily a result of an increase in employee costs, including salaries and wages and related costs, of approximately $2.7 million, primarily due to increased headcount. We also experienced increases in office expenses of $1.1 million, travel expenses of $1.1 million, marketing expenses of $828,000 and legal costs of $542,000. These increases were partially offset by a decrease in share-based compensation expense of approximately $827,000.
We expect our selling, general and administrative expenses to increase significantly in 2011 compared to 2010 as we continue to expand our sales and distribution capabilities as well as our administrative capabilities to support our overall corporate growth. We have and will continue to experience an increase in our employee headcount as well as an increase in costs associated with the necessary administrative infrastructure to support this expansion.
Research and Development
Research and development expenses are the direct and indirect costs associated with developing our products prior to commercialization and are expensed as incurred. These expenses fluctuate based on project level activity and consist primarily of salaries and wages and related employee costs of our research and development and clinical and regulatory staff, external research and development costs, and materials and expenses associated with clinical trials. Additional costs include travel, facilities and overhead allocations.
                                                 
    Three Months Ended June 30,     Six Months Ended June 30,  
(in thousands)   2011     2010     Change     2011     2010     Change  
Total research and development expenses
  $ 10,280     $ 7,511       37 %   $ 19,580     $ 12,267       60 %
The increase for the three months ended June 30, 2011 as compared to the three months ended June 30, 2010 was primarily due to an aggregate increase in costs associated with development projects, including animal studies, outside engineering, consumables, consultants and contractors, of $2.3 million, primarily related to MVAD development. We also experienced an increase in employee costs, including salaries and wages and related costs, of approximately $836,000 and an increase in non-cash share-based compensation of $271,000. These increases were partially offset by a decrease in costs associated with our U.S. clinical trials of $734,000, which have decreased subsequent to completion of enrollment of our BTT trial, with the exception of ongoing limited enrollment under a CAP.

 

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The increase for the six months ended June 30, 2011 as compared to the six months ended June 30, 2010 was primarily due to an increase in costs associated with development projects, including animal studies, outside engineering, consumables, consultants and contractors, of $4.2 million, primarily related to MVAD development. We also experienced an increase in employee costs, including salaries and wages and related costs, of approximately $1.5 million and an increase in share-based compensation of $621,000. Costs associated with our U.S. clinical trials increased by $275,000.
Even with commercial approval of the HeartWare System in Europe, we expect that research and development expenses will continue to represent a significant portion of our operating expenses for the foreseeable future related to clinical trials in the U.S. and new product development, including costs related to the development of the MVAD.
Foreign Exchange
We generate a substantial portion of our revenues and collect receivables in foreign currencies. Fluctuations in the exchange rate of the U.S. dollar against the Euro, British Pound and Australian dollar can result in foreign currency exchange gains and losses that may significantly impact our financial results. Continued fluctuation of these exchange rates could result in financial results that are not comparable from quarter to quarter. As discussed in Note 5, we entered into a foreign currency forward-exchange contract related to an asset purchase commitment by our Australian subsidiary. The purchase is denominated in a currency in which we do not normally transact business. Notwithstanding the aforementioned foreign currency forward-exchange contract, we do not currently utilize foreign currency contracts to mitigate foreign exchange gains and losses.
Net foreign exchange gains totaled approximately $134,000 and $726,000 in the three and six months ended June 30, 2011, respectively, compared to net losses of approximately $406,000 and $774,000 in the same periods of 2010. In 2011 and 2010, the majority of our realized and unrealized foreign exchange gains and losses were experienced upon the collection of certain accounts receivable that were denominated in foreign currencies, and the translation to U.S. dollars of customer accounts receivable denominated in foreign currencies at period end, primarily the Euro. We expect to continue realizing foreign exchange gains and losses for the foreseeable future as the majority of our sales denominated in foreign currencies are settled in Euros.
Interest Expense
Interest expense in 2011 consists of interest incurred on the principal amount of our convertible senior notes issued in December 2010, amortization of the related discount and amortization of the portion of the deferred financing costs allocated to the debt component. The convertible senior notes bear interest at a rate of 3.5% per annum. The discount on the convertible senior notes and the deferred financing costs are being amortized to interest expense through the December 15, 2017 maturity date of the convertible senior notes using the effective interest method.
Interest expense was approximately $2.65 million in the three months ended June 30, 2011. Interest incurred on the principal amount of the convertible notes at the 3.5% coupon rate was approximately $1.26 million and non-cash amortization of the discount and deferred financing costs totaled approximately $1.39 million.
Interest expense was approximately $5.25 million in the six months ended June 30, 2011. Interest incurred on the principal amount of the convertible notes at the 3.5% coupon rate was approximately $2.51 million and non-cash amortization of the discount and deferred financing costs totaled approximately $2.74 million.
Investment Income, net
Investment income is primarily derived from investments and cash and short-term deposit accounts held in the U.S. The amortization of premium on our investments is also included in investment income, net. Investment income, net was approximately $128,000 and $295,000 in the three and six months ended June 30, 2011 and 2010, respectively, compared to $161,000 and $273,000 in the same periods in the prior year. While we have had greater cash and investments balances during 2011 as a result of the issuance of our convertible senior notes in December 2010, we have experienced lower interest rates in 2011 compared to 2010.

 

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Income Taxes
We are subject to taxation in the United States and jurisdictions outside of the United States. These jurisdictions have different marginal tax rates. While we have incurred losses since inception, changes in issued capital and share ownership, as well as other factors, may limit our ability to utilize any net operating loss carry-forwards, and as such a 100% valuation allowance has been recorded against our net deferred tax assets.
As of June 30, 2011, we did not have revenues or profit which would be sufficient to allow any portion of our deferred tax assets to be recorded. We intend to monitor closely whether to record a deferred tax asset as we further expand the commercialization of our products.
Liquidity and Capital Resources
As of June 30, 2011, our cash and cash equivalents were approximately $118.8 million as compared to $192.1 million at December 31, 2010. The decrease is primarily a result of cash used to support our operating and investing activities and the purchase of short-term investments, partially offset by cash proceeds from the exercise of stock options.
Following is a summary of our cash flow activities:
                 
    Six Months Ended June 30,  
    2011     2010  
    (in thousands)  
Net cash used in operating activities
  $ (14,003 )   $ (9,279 )
Net cash used in investing activities
    (59,952 )     (19,426 )
Net cash provided by financing activities
    599       61,205  
Effect of exchange rate changes on cash and cash equivalents
    51       (9 )
 
           
Net (decrease) increase in cash and cash equivalents
  $ (73,305 )   $ 32,491  
 
           
Cash Used in Operating Activities
For the six months ended June 30, 2011, cash used in operating activities included a net loss of approximately $19.5 million and non-cash adjustments to net loss totaling approximately $11.0 million, which primarily consisted of $6.4 million of share-based compensation, $2.6 million for the amortization of the discount on our convertible notes and $1.1 million of depreciation and amortization. Also included in cash used in operating activities in the six months ended June 30, 2011 is approximately $7.5 million for the purchase and manufacture of inventories, $2.2 million for prepaid expenses and $555,000 for payment of trade accounts payable. These amounts were partially offset by net collections of trade accounts receivable of $3.5 million and an increase in accrued expenses of $1.3 million.
For the six months ended June 30, 2010, cash used in operating activities included a net loss of approximately $14.5 million, non-cash adjustments to net loss of approximately $7.1 million and changes in assets and liabilities of $1.8 million. Non-cash adjustments primarily consisted of share-based compensation of approximately $6.0 million and $628,000 of depreciation and amortization. Changes in assets and liabilities included a use of cash of approximately $6.8 million for the purchase and manufacture of inventories partially offset by $3.5 million in accounts receivable collections.

 

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Cash Used in Investing Activities
In the six months ended June 30, 2011, net cash used for the purchase (net of maturities in 2011) of available-for sale securities was $55.1 million compared to $16.6 million in the six months ended June 30, 2010. Other investing activities in the six months ended June 30, 2011 and 2010 used cash of approximately $4.9 million and $2.8 million, respectively. These amounts were expended to acquire property, plant and equipment and for capitalized patent costs.
Cash Provided by Financing Activities
In February 2010, we completed a public offering of approximately 1.77 million shares of our common stock, including the underwriter’s exercise of their over-allotment option to purchase 230,595 shares, at an offering price of $35.50 per share for aggregate gross proceeds of approximately $62.8 million. After fees and expenses, net proceeds from the offering were approximately $58.5 million. The offering was completed pursuant to a prospectus supplement, dated January 27, 2010, to a shelf registration statement previously filed with the SEC and which was declared effective on January 20, 2010. This shelf registration statement allows us to offer and sell from time to time, in one or more series or issuances and on terms that we will determine at the time of the offering, any combination of the securities described in the prospectus, up to an aggregate amount of $100 million.
The exercise of stock options in the six months ended June 30, 2011 and 2010 resulted in cash proceeds of approximately $600,000 and $2.8 million, respectively.
Operating Capital and Capital Expenditure Requirements
We have incurred operating losses to date and anticipate that we will continue to incur substantial net losses as we expand our sales and marketing capabilities, develop new products and seek regulatory approvals for the HeartWare System in the U.S. For the remainder of 2011, cash on hand is expected to primarily be used to fund our ongoing operations, including;
    expanding our sales and marketing capabilities on a global basis,
    continuing implants in the U.S. under a CAP and in our U.S. destination therapy clinical study,
    continued product development,
    regulatory activities, including PMA submissions and testing, and other compliance functions, and
    general working capital.
We expect to experience increased cash requirements for inventory and property related to the expansion of our manufacturing capabilities, including the build-out our new manufacturing facility located in Miami Lakes, Florida, to support continued growth.
Our convertible notes bear interest at a rate of 3.5% per annum, payable semi-annually in arrears on June 15 and December 15 of each year, beginning on June 15, 2011. During the quarter ended June 30, 2011 we paid the $2.5 million interest payment that was due on June 15, 2011. Based on the outstanding principal amount of our convertible senior notes at June 30, 2011, the semi-annual interest payment due on December 15, 2011 will be approximately $2.5 million. This amount is expected to be paid from cash on hand.
We believe cash on hand and investment balances as of June 30, 2011 are sufficient to support our planned operations throughout 2011 and 2012.

 

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Because of the numerous risks and uncertainties associated with the development of medical devices and the current economic situation, we are unable to estimate the exact amounts of capital outlays and operating expenditures necessary to obtain regulatory approvals in the U.S., fund commercial expansion outside of the U.S. and develop new products. Our future capital requirements will depend on many factors, including but not limited to the following:
    commercial acceptance of our products;
    costs to manufacture our products;
    expenses required to operate multiple clinical trials;
    further product research and development for next generation products and peripherals and expanding indications for our products as well as efforts to sustain and maintain incremental improvements to existing products;
    expanding our sales and marketing capabilities on a global basis, including building a team to support U.S. commercialization should the FDA approve our device for marketing in the U.S.;
    broadening our infrastructure in order to meet the needs of our growing operations; and
    complying with the requirements related to being a public company in both the United States and Australia.
Contractual Obligations
As of January 15, 2011, we entered into a Public, Private Partnership Agreement with the Regents of the University of Michigan whereby HeartWare, Inc. will act as industry sponsor of a study conducted by University of Michigan Cardiovascular Center and the University of Pittsburgh exploring the potential benefits of LVADs in patients who will be given earlier access to these devices under a grant awarded from the National Heart, Lung and Blood Institute. In the study, called REVIVE-IT, researchers will compare whether non-transplant eligible patients with heart failure less advanced than that of current LVAD recipients do better with implanted devices than with current medical therapy. Pursuant to the terms of the agreement, we have committed to provide financial support up to $9.6 million over the five-year term of the agreement.
Other than the financial commitment discussed above, in the six months ended June 30, 2011, there were no material changes to our contractual obligations provided in Part II, Item 7, Management’s Discussion and Analysis of Financial Condition and Results of Operations included in our 2010 Annual Report on Form 10-K filed with the SEC on February 24, 2011, outside the ordinary course of business.

 

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ITEM 3.   QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
Market risk represents the risk of changes in the value of market risk sensitive instruments caused by fluctuations in interest rates, foreign exchange rates and commodity prices. Changes in these factors could cause fluctuations in our results of operations and cash flows.
Interest Rate Risk
Our exposure to interest rate risk is currently confined to interest earnings on our cash and cash equivalents that are invested in highly liquid money market funds, short-term time deposits, short-term bank notes and short-term commercial paper. The primary objective of our investment activities is to preserve our capital to fund operations. We also seek to maximize income from our investments without assuming significant risk. We do not presently use derivative financial instruments in our investment portfolio. Our cash and investments policy emphasizes liquidity and preservation of principal over other portfolio considerations.
Our convertible senior notes do not bear interest rate risk as the notes were issued with a fixed interest rate of 3.5% per annum.
Foreign Currency Rate Fluctuations
We conduct business in foreign countries. For U.S. reporting purposes, we translate all assets and liabilities of our non-U.S. entities at the period-end exchange rate and revenues and expenses at the average exchange rates in effect during the periods. The net effect of these translation adjustments is shown in the accompanying condensed consolidated financial statements as a component of stockholders’ equity.
We generate a substantial portion of our revenues and collect receivables in foreign currencies. Fluctuations in the exchange rate of the U.S. dollar against the Euro, British Pound and Australian dollar can result in foreign currency exchange gains and losses that may significantly impact our financial results. These foreign currency transaction gains and losses are presented as a separate line item on our consolidated statements of operations. Continued fluctuation of these exchange rates could result in financial results that are not comparable from quarter to quarter. We do not currently utilize foreign currency contracts to mitigate the gains and losses generated by the remeasurement of non-functional currency assets and liabilities but do hold cash reserves in currencies in which those reserves are anticipated to be expended.
ITEM 4.   CONTROLS AND PROCEDURES
Evaluation of Disclosure Controls and Procedures
Our management, with the participation of the Chief Executive Officer and Chief Financial Officer, carried out an evaluation required by the Securities Exchange Act of 1934, as amended (the “Exchange Act”), of the effectiveness of the design and operation of our disclosure controls and procedures, as defined in Rule 13a-15(e) of the Exchange Act, as of June 30, 2011. Based on this evaluation, our Chief Executive Officer and Chief Financial Officer concluded that, as of June 30, 2011, our disclosure controls and procedures were effective to provide reasonable assurance that information required to be disclosed by us in the reports that we file or submit under the Exchange Act is recorded, processed, summarized, and reported within the time periods specified in the SEC’s rules and forms and to provide reasonable assurance that such information is accumulated and communicated to our management, including our Chief Executive Officer and Chief Financial Officer, as appropriate to allow timely decisions regarding required disclosures.

 

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Changes in Internal Control over Financial Reporting
There has been no change in our internal control over financial reporting during the three months ended June 30, 2011 that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.
Inherent Limitations on Controls and Procedures
Our management, including the Chief Executive Officer and Chief Financial Officer, does not expect that our disclosure controls and procedures or our internal control over financial reporting will prevent all errors and all fraud. A control system, no matter how well designed and operated, can provide only reasonable, not absolute, assurance that the control system’s objectives will be met. Further, the design of a control system must reflect the fact that there are resource constraints, and the benefits of controls must be considered relative to their costs. Because of the inherent limitations in all control systems, no evaluation of controls can provide absolute assurance that all control issues and instances of fraud, if any, have been detected. Thus, misstatements due to error or fraud may occur and not be detected. These inherent limitations include the realities that judgments in decision-making can be faulty, and that breakdowns can occur because of simple error or mistake. Additionally, controls can be circumvented by the individual acts of some persons, by collusion of two or more people, or by management override of controls.

 

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PART II. OTHER INFORMATION
ITEM 1.   LEGAL PROCEEDINGS
See Note 16 — Commitments and Contingencies
ITEM 1A.   RISK FACTORS
In addition to the information set forth in this report you should carefully consider the risk factors described in Part I, “Item 1A. Risk Factors” in our Annual Report on Form 10-K for the fiscal year ended December 31, 2010 filed with the SEC on February 24, 2011.
ITEM 2.   UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS
On February 2, 2010, we completed an underwritten public offering of 1,767,900 shares of our common stock (including 230,595 shares issued as a result of the full exercise of an overallotment option by the underwriter) at a price to the public of $35.50 per share, or an aggregate offering price of $62.8 million. The offer and sales of the shares in the offering were registered under the Securities Act of 1933 pursuant to a shelf registration statement on Form S-3 (File No. 333-164004), which became effective on January 20, 2010 and which registered up to $100 million of our common stock.
We raised approximately $58.5 million in the offering, after deducting underwriting discounts and commissions of $3.8 million and other estimated offering costs of $470,000. No payments were made by us to our directors, officers or persons owning ten percent or more of our common stock or to their associates, or to our affiliates. Through June 30, 2011, we have used approximately $43.5 million of the net proceeds of the offering, including approximately $13.6 million for the purchase of inventories, approximately $21.2 million for general working capital and approximately $8.7 million for purchases of property, plant and equipment.
ITEM 6.   EXHIBITS
         
  3.1    
Certificate of Incorporation of HeartWare International, Inc. (1)
       
 
  3.2    
Bylaws of HeartWare International, Inc. (1)
       
 
  10.35    
Third amendment to Business Lease, between HeartWare, Inc. and Atlantic-Philadelphia Realty LLC, dated June 30, 2011
       
 
  31.1    
Certification of Chief Executive Officer pursuant to Rule 13A-14(a) or Rule 15d-14(a) of the Securities Exchange Act
       
 
  31.2    
Certification of Chief Financial Officer pursuant to Rule 13A-14(a) or Rule 15d-14(a) of the Securities Exchange Act
       
 
  32.1    
Certification of Chief Executive Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
       
 
  32.2    
Certification of Chief Financial Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
 
     
(1)   Incorporated by reference to the respective exhibits filed with the Company’s Current Report on Form 8-K filed with the Securities and Exchange Commission on November 13, 2008.

 

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SIGNATURES
In accordance with the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
         
  HEARTWARE INTERNATIONAL, INC.
 
 
Date: August 5, 2011  /s/ Douglas Godshall    
  Douglas Godshall   
  Chief Executive Officer   
     
Date: August 5, 2011  /s/ David McIntyre    
  David McIntyre   
  Chief Financial Officer and Chief Operating Officer
(Principal Financial Officer) 
 
     
Date: August 5, 2011  /s/ Lauren Farrell    
  Lauren Farrell   
  Vice President, Finance (Principal Accounting Officer)   

 

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EXHIBIT INDEX
         
  10.35    
Third amendment to Business Lease, between HeartWare, Inc. and Atlantic-Philadelphia Realty LLC, dated June 30, 2011
       
 
  31.1    
Certification of Chief Executive Officer pursuant to Rule 13A-14(a) or Rule 15d-14(a) of the Securities Exchange Act
       
 
  31.2    
Certification of Chief Financial Officer pursuant to Rule 13A-14(a) or Rule 15d-14(a) of the Securities Exchange Act
       
 
  32.1    
Certification of Chief Executive Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
       
 
  32.2    
Certification of Chief Financial Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002

 

37

EX-10.35 2 c18306exv10w35.htm EXHIBIT 10.35 Exhibit 10.35
Exhibit 10.35
THIRD AMENDMENT TO LEASE
ATLANTIC-PHILADELPHIA REALTY LLC, LANDLORD
AND
HEARTWARE, INC., TENANT
This, Third Amendment to Lease (this “Third Amendment”), dated June 30, 2011, is entered into by and between ATLANTIC-PHILADELPHIA REALTY LLC, c/o Atlantic Management Corporation, 205 Newbury Street, Framingham, MA 01701, hereinafter referred to as “Landlord” and HEARTWARE, INC., a Delaware corporation, hereinafter referred to as “Tenant”.
WITNESSETH:
WHEREAS, Tenant and Landlord executed a lease dated December 27, 2006 (the “Initial Lease”), of certain premises situated on the first floor of the building and referenced as Suite 101 (the “Original Premises”), located at 205 Newbury Street, Framingham, Massachusetts ( the “Building”); and
WHEREAS, the Initial Lease was amended by the First Amendment to Lease dated August 19, 2008 (the “First Amendment”), by replacement of the Original Premises with new space located on the First Floor of the Building, referred to as Suite 103 and Suite 104 as shown on Exhibit B-1 attached to and incorporated into the First Amendment, (the “Relocation Premises”) as shown on Exhibit A-1, attached to the First Amendment to the Lease; and
WHEREAS, the Initial Lease was further amended by the Second Amendment to Lease dated August 9, 2010 (the “Second Amendment”), by re-leasing the Original Premises, together with additional premises located on the second floor of the Building known as Suite 204 (the “Expansion Premises”) which together with the Initial Lease, the First Amendment, are hereinafter referred to as the “Lease”; and

 

 


 

WHEREAS, the Tenant has requested and the Landlord agrees to lease to the Tenant additional space on the second floor totaling 2,760 sq ft (Suite 202 — hereinafter “Additional Space” under the Lease; and
WHEREAS, the Landlord and Tenant have agreed to amend the defined terms and other sections of the Lease to reflect certain agreements relating to the Premises, Rent, Tenant Improvements, Security Deposit, Base Year for Operating and Tax Expenses regarding the Additional Space within the building, all as hereinafter set forth;
NOW THEREFORE, in consideration of the foregoing and for other good and valuable consideration, the receipt and sufficiency of which is hereby acknowledged, the parties agree as follows:
1. Effective Date. This Third Amendment shall be effective as of the Rent and Term Commencement Date, defined in Paragraph 2(c) below.
2. Amendment of Article 1 of the Lease — Section 1.1. Section 1.1 of the Lease is hereby amended as follows:
a. The term “TENANT SPACE” is hereby amended by adding the Additional Space Premises, as previously defined.
b. The subject “RENTABLE FLOOR AREA OF TENANT SPACE” is hereby amended by adding 2,760 rentable square feet, being the Additional Space.
c. The subject “RENT AND TERM COMMENCEMENT DATE” is hereby amended by adding (i) relative to the Additional Space, the date of August 1, 2011, noting that Landlord has agreed to provide Tenant with early access to these premises at least fourteen (14) days’ prior to the Rent and Term Commencement Date for the purpose of installation of furniture systems, equipment, telephone, data and similar items.

 

 


 

d. The subject “TERM” is hereby amended with respect to the Additional Space as follows: Beginning on the Rent and Term Commencement Date (as that date pertains to each space) and terminating December 31, 2014.
e. The subject “TENANT’S PROPORTIONATE SHARE” is hereby amended by deleting reference to “12.38%” and replacing it with “31.28%, which percentage shall be effective on the Rent and Term Commencement Date with respect to the Additional Space, 4.85% ; which percentage shall be effective on the Rent and Term Commencement Date with respect to Relocation Premises, 12.38%, which percentage shall be effective on the Rent and Term Commencement Date with respect to the Expansion Premises, 7.85%, which percentage shall be effective on the Rent and Term Commencement Date with respect to the original Premises, 6.2%, “
f. The subject BASE YEAR FOR CALCULATING LANDLORD’S OPERATING EXPENSES” is hereby amended by adding the following: “Relative to the Additional Space the Base Year for calculating Landlord’s Operating Expenses shall be 2011.”
g. The subject REAL ESTATE TAX BASE YEARis hereby amended by adding the following: “Relative to the Additional Space the Real Estate Tax Base Year shall be 2012.”

 

 


 

h. The subject “ANNUAL BASE RENT” is hereby amended by adding to the schedule set forth in the Second Amendment the following:
(iv) For the Additional Space, $17.50 per rentable square foot from August 1, 2011 and then $18.00 per rentable square foot from August 1, 2012 through December 31, 2014;
i. The subject “SECURITY DEPOSIT” is hereby amended by adding the following: “Tenant shall deposit the sum equal to one month’s rent for the Additional Space, which shall be held along with the initial Security Deposit of $6,324.58 in a non-interest bearing account.”
j. The subject “PARKING” is hereby amended by deleting “Tenant will receive 3.8 parking spaces per 1,000 square feet rented, being 57 spaces, on a first-come, first-served basis” and substituting therefore the following: “Tenant will receive 3.8 parking spaces per 1,000 square feet rented, being 67 spaces, on a first-come, first-served basis”.
3. Further Amendment of Article 1 of the Lease. Section 1.2 Exhibits is hereby amended by adding Exhibit B-4, showing the Additional Space.
4. Tenant Improvements. Per Exhibit A hereto and at Landlord’s expense, Landlord does hereby agree to complete the following improvements: (i) a new Kitchen by providing 3 rows of adjustable shelves on the Kitchen Wall; install new cabinets and counter tops; provide plumbing; water heater, drains, sinks and faucet (ii) add a 3’ X 6’ glass side light to allow natural light into the Kitchen; (iii) Paint and carpet entire suite (except VCT in Kitchen area); and (iv) other alterations reflected in the floor plan attached as Exhibit A.

 

 


 

5. Brokers. Landlord shall be responsible for the payment of all brokerage fees due to R. W. Holmes Realty (“Holmes”) in connection with this Third Amendment pursuant to a separate agreement between Landlord and Holmes.
[Remainder of this page intentionally left blank.]

 

 


 

6. No Other Amendments. Except as otherwise provided herein, the Lease is hereby ratified and confirmed and shall remain unmodified and in full force and effect.
Executed as a sealed instrument by the duly authorized signatories of the parties hereto in two or more counterparts as of the day and year first above written.
                             
LANDLORD:       TENANT:    
 
                           
ATLANTIC-PHILADELPHIA REALTY, LLC       HEARTWARE, INC.    
By its Managing Agent,                    
Atlantic Management Corporation                    
 
                           
By:   /s/ David Capabianco       By:   /s/ Lawrence J. Knopf    
                     
 
  Its:   COO           Its:   SVP/General Counsel    

 

 


 

Exhibit A — Tenant Improvements Plan

 

 

EX-31.1 3 c18306exv31w1.htm EXHIBIT 31.1 Exhibit 31.1
Exhibit 31.1
CERTIFICATION OF CHIEF EXECUTIVE OFFICER PURSUANT TO RULE 13A-14(a) OR RULE 15d-14(a)
OF THE SECURITIES EXCHANGE ACT OF 1934
I, Douglas Godshall, certify that:
1.   I have reviewed this Quarterly Report on Form 10-Q of HeartWare International, Inc.;
2.   Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;
3.   Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;
4.   The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:
  a)   Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;
  b)   Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;
  c)   Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and
  d)   Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and
5.   The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions):
  a)   All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
  b)   Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.
Date: August 5, 2011
         
  /s/ Douglas Godshall    
  Douglas Godshall   
  Chief Executive Officer
(Principal Executive Officer) 
 

 

 

EX-31.2 4 c18306exv31w2.htm EXHIBIT 31.2 Exhibit 31.2
Exhibit 31.2
CERTIFICATION OF CHIEF FINANCIAL OFFICER PURSUANT TO RULE 13A-14(a) OR RULE 15d-14(a)
OF THE SECURITIES EXCHANGE ACT OF 1934
I, David McIntyre, certify that:
1.   I have reviewed this Quarterly Report on Form 10-Q of HeartWare International, Inc.;
2.   Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;
3.   Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;
4.   The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:
  a)   Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;
  b)   Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;
  c)   Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and
  d)   Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and
5.   The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions):
  a)   All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
  b)   Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.
Date: August 5, 2011
         
  /s/ David McIntyre    
  David McIntyre   
  Chief Financial Officer
(Principal Financial Officer) 
 

 

 

EX-32.1 5 c18306exv32w1.htm EXHIBIT 32.1 Exhibit 32.1
Exhibit 32.1
CERTIFICATION OF CHIEF EXECUTIVE OFFICER PURSUANT TO 18 U.S.C.
SECTION 1350 AS ADOPTED PURSUANT TO SECTION 906 OF THE
SARBANES-OXLEY ACT OF 2002
In connection with the Quarterly Report on Form 10-Q of HeartWare International, Inc. (the “Company”) for the quarterly period ended June 30, 2011 as filed with the Securities and Exchange Commission on the date hereof (the “Report”), the undersigned Chief Executive Officer of the Company hereby certifies, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, that based on his knowledge:
(1)  
the Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended; and
(2)  
the information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.
Date: August 5, 2011
         
  /s/ Douglas Godshall    
  Douglas Godshall   
  Chief Executive Officer
(Principal Executive Officer) 
 

 

 

EX-32.2 6 c18306exv32w2.htm EXHIBIT 32.2 Exhibit 32.2
Exhibit 32.2
CERTIFICATION OF CHIEF FINANCIAL OFFICER PURSUANT TO 18 U.S.C.
SECTION 1350 AS ADOPTED PURSUANT TO SECTION 906 OF THE
SARBANES-OXLEY ACT OF 2002
In connection with the Quarterly Report on Form 10-Q of HeartWare International, Inc. (the “Company”) for the quarterly period ended June 30, 2011 as filed with the Securities and Exchange Commission on the date hereof (the “Report”), the undersigned Chief Financial Officer of the Company hereby certifies, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, that based on his knowledge:
(1)  
the Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended; and
(2)  
the information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.
Date: August 5, 2011
         
  /s/ David McIntyre    
  David McIntyre   
  Chief Financial Officer
(Principal Financial Officer) 
 

 

 

EX-101.INS 7 htwr-20110630.xml EX-101 INSTANCE DOCUMENT 0001389072 2011-07-27 0001389072 2011-06-30 0001389072 2010-12-31 0001389072 2011-04-01 2011-06-30 0001389072 2010-04-01 2010-06-30 0001389072 2011-01-01 2011-06-30 0001389072 2010-01-01 2010-06-30 0001389072 us-gaap:CommonStockMember 2010-12-31 0001389072 us-gaap:AdditionalPaidInCapitalMember 2010-12-31 0001389072 us-gaap:RetainedEarningsMember 2010-12-31 0001389072 us-gaap:AccumulatedOtherComprehensiveIncomeMember 2010-12-31 0001389072 us-gaap:CommonStockMember 2011-01-01 2011-06-30 0001389072 us-gaap:AdditionalPaidInCapitalMember 2011-01-01 2011-06-30 0001389072 us-gaap:RetainedEarningsMember 2011-01-01 2011-06-30 0001389072 us-gaap:AccumulatedOtherComprehensiveIncomeMember 2011-01-01 2011-06-30 0001389072 us-gaap:CommonStockMember 2011-06-30 0001389072 us-gaap:AdditionalPaidInCapitalMember 2011-06-30 0001389072 us-gaap:RetainedEarningsMember 2011-06-30 0001389072 us-gaap:AccumulatedOtherComprehensiveIncomeMember 2011-06-30 0001389072 2009-12-31 0001389072 2010-06-30 iso4217:USD xbrli:shares xbrli:shares iso4217:USD HeartWare International, Inc. 0001389072 --12-31 Yes No Yes Accelerated Filer 10-Q false 2011-06-30 Q2 2011 13925984 118843674 192148312 79998132 21330110 15248062 19052672 22522356 15076590 4659251 2406505 241271475 250014189 11130352 7484022 0 4005659 1785509 1595456 2800497 2939149 1538429 1538429 258526262 267576904 3336590 3889643 8331089 7001350 11667679 10890993 91518710 88921557 0 0 .001 .001 5000000 5000000 0 0 0 0 13926 13879 .001 .001 25000000 25000000 13925984 13878686 13925984 13878686 309569724 302533344 -146795591 -127268545 -7457261 -7548706 9075 34382 -7448186 -7514324 155339873 167764354 258526262 267576904 20389491 9757078 38364091 20460198 7913346 4293348 15508799 9973890 12476145 5463730 22855292 10486308 9892325 7688379 18556413 12244801 10279529 7511201 19579657 12266879 20171854 15199580 38136070 24511680 -7695709 -9735850 -15280778 -14025372 133889 -406486 726214 -773500 2646558 971 5252030 971 127902 161258 295100 273479 -15552 -15552 -10096028 -9982049 -19527046 -14526364 -10096028 -9982049 -19527046 -14526364 -0.73 -0.73 -1.40 -1.09 13923258 13682734 13911993 13322531 64938 -139455 91445 -62738 7751 -21332 -25307 -45124 -10023339 -10142836 -19460908 -14634226 13878686 13879 302533344 -127268545 -7514324 47298 47 599567 599614 6436813 6436813 -19527046 91445 -25307 13925984 13926 309569724 -146795591 -7448186 1019609 580536 63887 47862 6436813 5998962 440507 167056 2597153 139252 -340100 -284998 -3526642 -3528615 7547061 6757485 2247717 389974 -554869 356854 1309423 1430473 -14003307 -9278467 80128177 16644600 -25000000 4667787 2497481 253940 283410 98225 -59951679 -19425491 62760450 600 4359934 599614 2804101 599014 61204617 51334 -9402 -73304638 32491257 50834714 83325971 <!--DOCTYPE html PUBLIC "-//W3C//DTD XHTML 1.0 Transitional//EN" "http://www.w3.org/TR/xhtml1/DTD/xhtml1-transitional.dtd" --> <!-- Begin Block Tagged Note 1 - us-gaap:OrganizationConsolidationAndPresentationOfFinancialStatementsDisclosureTextBlock--> <div align="left" style="font-family: 'Times New Roman',Times,serif; margin-left: 0in; "> <!-- xbrl,ns --> <!-- xbrl,nx --> <div align="center" style="font-size: 10pt; margin-top: 0pt"><b> </b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt"><b>Note 1. Basis of Presentation</b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">HeartWare International, Inc., referred to in these notes collectively with its subsidiaries HeartWare Pty. Limited, HeartWare, Inc., HeartWare (UK)&#160;Limited and HeartWare GmbH as &#8220;we,&#8221; &#8220;our,&#8221; &#8220;HeartWare&#8221; or the &#8220;Company,&#8221; is a medical device company that develops and manufactures small implantable heart pumps, or ventricular assist devices, used in the treatment of advanced heart failure. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">The accompanying unaudited interim condensed consolidated financial statements have been prepared pursuant to the rules and regulations of the Securities and Exchange Commission (&#8220;SEC&#8221;) for reporting of interim financial information. Pursuant to such rules and regulations, certain information and footnote disclosures normally included in financial statements prepared in accordance with accounting principles generally accepted in the United States have been condensed or omitted. Accordingly, these statements do not include all the disclosures normally required by accounting principles generally accepted in the United States for annual financial statements and should be read in conjunction with Management&#8217;s Discussion and Analysis of Financial Condition and Results of Operations contained in this report and the audited financial statements and notes thereto for the year ended December&#160;31, 2010 included in our Annual Report on Form 10-K. The accompanying condensed consolidated balance sheet as of December&#160;31, 2010 has been derived from our audited financial statements. The condensed consolidated statements of operations for the three and six months ended June&#160;30, 2011 and cash flows for the six months ended June&#160;30, 2011 are not necessarily indicative of the results to be expected for any future period or for the year ending December&#160;31, 2011. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">In the opinion of management, the accompanying unaudited interim condensed consolidated financial statements contain all adjustments (consisting of only normally recurring adjustments) necessary to present fairly the financial position and results of operations as of the dates and for the periods presented. </div> </div> <!--DOCTYPE html PUBLIC "-//W3C//DTD XHTML 1.0 Transitional//EN" "http://www.w3.org/TR/xhtml1/DTD/xhtml1-transitional.dtd" --> <!-- Begin Block Tagged Note 2 - htwr:LiquidityDisclosuresTextBlock--> <div align="left" style="font-family: 'Times New Roman',Times,serif; margin-left: 0in; "> <div align="left" style="font-size: 10pt; margin-top: 10pt"><b>Note 2. Liquidity</b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">At June&#160;30, 2011, we had approximately $198.8&#160;million of cash, cash equivalents and investments. The accompanying condensed consolidated financial statements have been prepared in conformity with accounting principles generally accepted in the United States, which contemplates continuation of the Company as a going concern. We have sustained substantial losses from operations since our inception, and such losses have continued through June&#160;30, 2011. At June&#160;30, 2011, we had an accumulated deficit of approximately $146.8&#160;million. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">We have financed our operations primarily through the issuance of shares of our common stock and the issuance of convertible notes. Most recently, in December&#160;2010, we consummated the issuance and sale of $143.75&#160;million aggregate principal amount of convertible notes. The convertible notes are the senior unsecured obligations of the Company. The convertible notes bear interest at a rate of 3.5% per annum, payable semi-annually in arrears on June&#160;15 and December&#160;15 of each year, beginning on June&#160;15, 2011. The convertible notes will mature on December&#160;15, 2017, unless earlier repurchased or converted. The convertible notes will be convertible at an initial conversion rate of 10 shares of common stock per $1,000 principal amount of convertible notes, which corresponds to an initial conversion price of $100.00 per share of common stock. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">For the remainder of 2011, our cash, cash equivalents and investments are expected to primarily be used to fund our ongoing operations including expanding our sales and marketing capabilities on a global basis, continuing our ENDURANCE trial for destination therapy, enrolling additional patients in our ADVANCE trial under a Continued Access Protocol (&#8220;CAP&#8221;), continued product development, regulatory and other compliance functions, including costs related to testing and submission of our PMA application, as well as for general working capital. We believe our cash, cash equivalent and investment balances are sufficient to support our planned operations through 2012. </div> <!-- Folio --> <!-- /Folio --> </div> <!-- PAGEBREAK --> <div style="font-family: 'Times New Roman',Times,serif; margin-left: 0in; "> </div> <!--DOCTYPE html PUBLIC "-//W3C//DTD XHTML 1.0 Transitional//EN" "http://www.w3.org/TR/xhtml1/DTD/xhtml1-transitional.dtd" --> <!-- Begin Block Tagged Note 3 - us-gaap:SignificantAccountingPoliciesTextBlock--> <div style="font-family: 'Times New Roman',Times,serif; margin-left: 0in; "> <div align="left" style="font-size: 10pt; margin-top: 10pt"><b>Note 3. Significant Accounting Policies</b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; margin-left: 4%"><b><i>Principles of Consolidation</i></b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">The condensed consolidated financial statements include the accounts of HeartWare International, Inc., and its subsidiaries described in Note 1. All inter-company balances and transactions have been eliminated in consolidation. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; margin-left: 4%"><b><i>Accounting Estimates</i></b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">The preparation of consolidated financial statements in conformity with accounting principles generally accepted in the United States (&#8220;US GAAP&#8221;) requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities, the disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting periods. Actual results could differ from those estimates. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; margin-left: 4%"><b><i>Cash and Cash Equivalents</i></b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">Cash and cash equivalents are recorded in the condensed consolidated balance sheets at cost, which approximates fair value. All highly liquid investments with an original maturity of three months or less at the date of purchase are considered to be cash equivalents. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; margin-left: 4%"><b><i>Investments</i></b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">Our investments classified as available-for-sale are stated at fair value with unrealized gains and losses reported in accumulated other comprehensive loss within stockholders&#8217; equity. We classify our available-for-sale investments as short-term if their remaining time to maturity at purchase is beyond three months. Investments with maturities beyond one year may be classified as short-term based on their highly liquid nature and because such marketable securities represent the investment of cash that is available for current operations. Interest on investments classified as available-for-sale is included in investment income, net. Premiums paid on our short-term investments are amortized over the remaining term of the investment and such amortization is included in investment income, net. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; margin-left: 4%"><b><i>Receivables</i></b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">Accounts receivable consists of amounts due from the sale of our HeartWare<sup style="font-size: 85%; vertical-align: text-top">&#174;</sup> Ventricular Assist System (the &#8220;HeartWare System&#8221;) to our customers, which include hospitals, health research institutions and medical device distributors. Our receivables are geographically dispersed, with a significant portion from customers located in Europe and other foreign countries. As of June&#160;30, 2011 and December&#160;31, 2010, one customer had an accounts receivable balance representing approximately 11% and 13%, respectively, of our total accounts receivable. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">We maintain allowances for doubtful accounts for estimated losses that may result from an inability to collect payments owed to us for product sales. We regularly review the allowance by considering factors such as historical experience, the age of the accounts receivable balances and current economic conditions that may affect a customer&#8217;s ability to pay. </div> <!-- Folio --> <!-- /Folio --> </div> <!-- PAGEBREAK --> <div style="font-family: 'Times New Roman',Times,serif; margin-left: 0in; "> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">The following table summarizes the change in our allowance for doubtful accounts for the six months ended June&#160;30, 2011 and 2010: </div> <div align="center"> <table style="font-size: 10pt; text-align: left" cellspacing="0" border="0" cellpadding="0" width="100%"> <!-- Begin Table Head --> <tr valign="bottom"> <td width="72%">&#160;</td> <td width="3%">&#160;</td> <td width="1%">&#160;</td> <td width="9%">&#160;</td> <td width="1%">&#160;</td> <td width="3%">&#160;</td> <td width="1%">&#160;</td> <td width="9%">&#160;</td> <td width="1%">&#160;</td> </tr> <tr style="font-size: 10pt" valign="bottom"> <td>&#160;</td> <td>&#160;</td> <td nowrap="nowrap" align="center" colspan="6"><b>Six months ended</b></td> <td>&#160;</td> </tr> <tr style="font-size: 10pt" valign="bottom"> <td>&#160;</td> <td>&#160;</td> <td nowrap="nowrap" align="center" colspan="6" style="border-bottom: 1px solid #000000"><b>June 30,</b></td> <td>&#160;</td> </tr> <tr style="font-size: 10pt" valign="bottom"> <td>&#160;</td> <td>&#160;</td> <td nowrap="nowrap" align="center" colspan="2" style="border-bottom: 1px solid #000000"><b>2011</b></td> <td>&#160;</td> <td>&#160;</td> <td nowrap="nowrap" align="center" colspan="2" style="border-bottom: 1px solid #000000"><b>2010</b></td> <td>&#160;</td> </tr> <!-- End Table Head --> <!-- Begin Table Body --> <tr valign="bottom" style="background: #cceeff"> <td> <div style="margin-left:15px; text-indent:-15px">Beginning balance </div></td> <td>&#160;</td> <td align="left">$</td> <td align="right">600,000</td> <td>&#160;</td> <td>&#160;</td> <td align="left">$</td> <td align="right">&#8212;</td> <td>&#160;</td> </tr> <tr valign="bottom"> <td> <div style="margin-left:15px; text-indent:-15px">Additions (bad debt expense) </div></td> <td>&#160;</td> <td>&#160;</td> <td align="right">300,000</td> <td>&#160;</td> <td>&#160;</td> <td>&#160;</td> <td align="right">285,000</td> <td>&#160;</td> </tr> <tr valign="bottom" style="background: #cceeff"> <td> <div style="margin-left:15px; text-indent:-15px">Deductions (charge-offs) </div></td> <td>&#160;</td> <td>&#160;</td> <td align="right">&#8212;</td> <td>&#160;</td> <td>&#160;</td> <td>&#160;</td> <td align="right">&#8212;</td> <td>&#160;</td> </tr> <tr style="font-size: 1px"> <td> <div style="margin-left:15px; text-indent:-15px">&#160; </div></td> <td>&#160;</td> <td nowrap="nowrap" colspan="2" align="right" style="border-top: 1px solid #000000">&#160;</td> <td>&#160;</td> <td>&#160;</td> <td nowrap="nowrap" colspan="2" align="right" style="border-top: 1px solid #000000">&#160;</td> <td>&#160;</td> </tr> <tr valign="bottom"> <td> <div style="margin-left:15px; text-indent:-15px">Ending balance </div></td> <td>&#160;</td> <td align="left">$</td> <td align="right">900,000</td> <td>&#160;</td> <td>&#160;</td> <td align="left">$</td> <td align="right">285,000</td> <td>&#160;</td> </tr> <tr style="font-size: 1px"> <td> <div style="margin-left:15px; text-indent:-15px">&#160; </div></td> <td>&#160;</td> <td nowrap="nowrap" colspan="2" align="right" style="border-top: 3px double #000000">&#160;</td> <td>&#160;</td> <td>&#160;</td> <td nowrap="nowrap" colspan="2" align="right" style="border-top: 3px double #000000">&#160;</td> <td>&#160;</td> </tr> <!-- End Table Body --> </table> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; margin-left: 4%">As of June&#160;30, 2011 and December&#160;31, 2010, we did not have an allowance for returns. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; margin-left: 4%"><b><i>Inventories, net</i></b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">Inventories are stated at the lower of cost or market. Cost is determined using a first-in, first-out, or FIFO, method. Work-in-process and finished goods include direct and indirect labor and manufacturing overhead. Finished goods include product which is ready-for-use and which is held by us or by our customers on a consignment basis. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">We review our inventory for excess or obsolete inventory and write-down obsolete or otherwise unmarketable inventory to its estimated net realizable value. Obsolescence may occur due to product expiring or product improvements rendering previous versions obsolete. In May&#160;2011, we began shipping a sintered version of the HeartWare System on a global basis. Sintering is commonly used in medical devices to facilitate tissue adhesion. The extent to which this product enhancement will cause obsolescence of existing non-sintered inventory is difficult to determine because the rate of product adoption of sintered product is dependent on individual customer acceptance, implantation rates and approval timeframes of Institutional Review Boards at U.S. sites. As of June 30, 2011, we had $3.5&#160;million of non-sintered inventory on hand and this product continues to be implanted at customer sites. 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Investments are considered available-for-sale as of June&#160;30, 2011 and December&#160;31, 2010 and are carried at fair value. See Note 6, &#8220;Fair Value Measurements&#8221; and Note 10, &#8220;Debt&#8221; for more information. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; margin-left: 4%"><b><i>Vendor Concentration</i></b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">For the three and six months ended June&#160;30, 2011, we purchased approximately 55% of our inventory components and supplies from two vendors. For the three and six months ended June&#160;30, 2010, we purchased approximately 62% and 51%, respectively, of our inventory components and supplies from the same two vendors. In addition, one of these vendors supplies consulting services and material used in research and development activities. As of June&#160;30, 2011 and 2010, the amounts due to these vendors totaled approximately $788,000 and $1.1&#160;million, respectively. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; margin-left: 4%"><b><i>Concentration of Credit Risk and other Risks and Uncertainties</i></b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">Financial instruments that potentially expose us to concentrations of credit risk consist primarily of cash and cash equivalents, investments and trade accounts receivable. Cash and cash equivalents are primarily on deposit with financial institutions in the United States and these deposits generally exceed the amount of insurance provided by the Federal Deposit Insurance Corporation (the &#8220;FDIC&#8221;). The Company has not experienced any historical losses on its deposits of cash and cash equivalents. Our investments consist of investment grade rated corporate and government agency debt. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">Concentration of credit risk with respect to our trade accounts receivable from our customers is primarily limited to hospitals, health research institutions and medical device distributors. Credit is extended to our customers, based on an evaluation of a customer&#8217;s financial condition and collateral is not required. To date, we have not experienced any credit losses, but have established an allowance for doubtful accounts of $900,000 at June&#160;30, 2011. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">We are subject to certain risks and uncertainties including, but not limited to, our ability to achieve profitability, to generate cash flow sufficient to satisfy our indebtedness, to run clinical trials in order to receive and maintain FDA and foreign regulatory approvals for our products, the ability to achieve widespread acceptance of our product, our ability to manufacture our products in a sufficient volume and at a reasonable cost, the ability to protect our proprietary technologies and develop new products, the risks associated with operating in foreign countries, and general competitive and economic conditions. Changes in any of the preceding areas could have a material adverse effect on our business, results of operations or financial position. </div> <!-- Folio --> <!-- /Folio --> </div> <!-- PAGEBREAK --> <div style="font-family: 'Times New Roman',Times,serif; margin-left: 0in; "> <div align="left" style="font-size: 10pt; margin-top: 10pt; margin-left: 4%"><b><i>New Accounting Standards</i></b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">In May&#160;2011, the Financial Accounting Standards Board (FASB)&#160;issued Accounting Standards Update (ASU)&#160;No.&#160;2011-04, <i>Fair Value Measurement (Topic 820): Amendments to Achieve Common Fair Value Measurement and Disclosure Requirements in U.S. GAAP and IFRSs</i>. ASU No.&#160;2011-04 clarifies some existing concepts, eliminates wording differences between U.S. GAAP and International Financial Reporting Standards (&#8220;IFRS&#8221;), and in some limited cases, changes some principles to achieve convergence between U.S. GAAP and IFRS. ASU No.&#160;2011-04 results in a consistent definition of fair value and common requirements for measurement of and disclosure about fair value between U.S. GAAP and IFRS. ASU No.&#160;2011-04 also expands the disclosures for fair value measurements that are estimated using significant unobservable (Level 3) inputs. The provisions of ASU No.&#160;2011-04 will become effective for us on January&#160;1, 2012 and are to be applied prospectively. We do not expect the adoption of the provisions of ASU No.&#160;2011-04 to have a material effect on our consolidated financial position, results of operations or cash flows and we do not expect to materially modify or expand our financial statement footnote disclosures. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">In June&#160;2011, the FASB issued ASU No.&#160;2011-05, <i>Comprehensive Income (Topic 220): Presentation of Comprehensive Income</i>. ASU No.&#160;2011-05 requires an entity to present the total of comprehensive income, the components of net income, and the components of other comprehensive income either in a single continuous statement of comprehensive income, or in two separate but consecutive statements. ASU No.&#160;2011-05 eliminates the option to present components of other comprehensive income as part of the statement of stockholders&#8217; equity. The presentation requirements will become effective for us on January&#160;1, 2012. As ASU No.&#160;2011-05 applies to financial statement presentation matters, the adoption of ASU No.&#160;2011-05 will not affect our consolidated financial position, results of operations or cash flows and we believe our current presentation of comprehensive income complies with the new presentation requirements. </div> </div> <!--DOCTYPE html PUBLIC "-//W3C//DTD XHTML 1.0 Transitional//EN" "http://www.w3.org/TR/xhtml1/DTD/xhtml1-transitional.dtd" --> <!-- Begin Block Tagged Note 4 - us-gaap:InvestmentsInDebtAndMarketableEquitySecuritiesAndCertainTradingAssetsDisclosureTextBlock--> <div style="font-family: 'Times New Roman',Times,serif; margin-left: 0in; "> <div align="left" style="font-size: 10pt; margin-top: 10pt"><b>Note 4. 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Foreign Exchange Instruments</b> </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">During the quarter ended June&#160;30, 2011, we entered into a foreign currency forward-exchange contract in an effort to minimize the risk of future fluctuations in the exchange rates between Australian dollars and Japanese Yen. The foreign currency forward-exchange contract was directly related to an asset purchase commitment by our Australian subsidiary. We do not utilize derivative financial instruments for speculative or trading purposes. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">As of June&#160;30, 2011, the forward contract to sell Australian dollars to Japanese Yen had a notional value of AU$858,000 and an exchange rate of one Australian dollar to 83.35 Japanese Yen. 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The Convertible Notes will mature on December&#160;15, 2017, unless earlier repurchased by us or converted. </div> <!-- Folio --> <!-- /Folio --> </div> <!-- PAGEBREAK --> <div style="font-family: 'Times New Roman',Times,serif; margin-left: 0in; "> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">The Convertible Notes will be convertible at an initial conversion rate of 10 shares of our common stock per $1,000 principal amount of Convertible Notes, which corresponds to an initial conversion price of $100.00 per share of our common stock representing a conversion premium of approximately 23% based on the closing price of $81.31 per share of our common stock on December&#160;9, 2010, the day the notes were priced. The conversion rate is subject to adjustment from time to time upon the occurrence of certain events. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">Prior to June&#160;15, 2017, holders may convert their Convertible Notes at their option only upon satisfaction of one or more conditions relating to the sale price of our common stock, the trading price per $1,000 principal amount of Convertible Notes or specified corporate events. On or after June&#160;15, 2017, until the close of business of the business day immediately preceding the date the Convertible Notes mature, holders may convert their Convertible Notes at any time, regardless of whether any of the foregoing conditions have been met. As of the date of this report, none of the events that would allow holders to convert their Convertible Notes have occurred. Upon conversion, we will pay or deliver, as the case may be, cash, shares of our common stock or a combination thereof, at our election. </div> <div align="left" style="font-size: 10pt; margin-top: 10pt; text-indent: 4%">In accordance with ASC 470-20, <i>Debt</i>, which applies to certain convertible debt instruments that may be settled in cash or other assets, or partially in cash, upon conversion, we recorded the long-term debt and equity components on our Convertible Notes separately on the issuance date. The amount recorded for long-term debt was determined by measuring the fair value of a similar liability that does not have an associated equity component. The measurement of fair value required the Company to make estimates and assumptions to determine the present value of the cash flows of the Convertible Notes, absent the conversion feature. 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We receive a tax deduction for certain stock option exercises during the period the options are exercised, and for the vesting of restricted stock units during the period the restricted stock units vest. For stock options, the amount of the tax deduction is generally for the excess of the fair market value of our shares of common stock over the exercise price of the stock options at the date of exercise. For restricted stock units, the amount of the tax deduction is generally for the fair market value of our shares of common stock at the vesting date. 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These holders requested various financial and other information regarding HeartWare, Inc. for the purpose of determining the Company&#8217;s compliance with their rights as holders of Series&#160;A Preferred Stock, including whether a liquidation event has occurred since inception in 2003. HeartWare, Inc. issued Series&#160;A-1 and Series&#160;A-2 Preferred Stock to certain equity holders of Kriton Medical, Inc. when HeartWare, Inc. purchased substantially all of the assets of Kriton in July&#160;2003. The Series&#160;A-1 and Series A-2 Preferred Stock do not have voting or dividend rights but entitle the holders thereof to receive, upon certain liquidation events of HeartWare, Inc. (but not the liquidation of or change of control of HeartWare International, Inc.), an amount equal to $10 per share of Series&#160;A-1 and $21 per share of Series&#160;A-2. 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Condensed Consolidated Statements of Operations (Unaudited) (USD $)
3 Months Ended 6 Months Ended
Jun. 30, 2011
Jun. 30, 2010
Jun. 30, 2011
Jun. 30, 2010
Condensed Consolidated Statements of Operations [Abstract]        
Revenues, net $ 20,389,491 $ 9,757,078 $ 38,364,091 $ 20,460,198
Cost of revenues 7,913,346 4,293,348 15,508,799 9,973,890
Gross profit 12,476,145 5,463,730 22,855,292 10,486,308
Operating expenses:        
Selling, general and administrative 9,892,325 7,688,379 18,556,413 12,244,801
Research and development 10,279,529 7,511,201 19,579,657 12,266,879
Total operating expenses 20,171,854 15,199,580 38,136,070 24,511,680
Loss from operations (7,695,709) (9,735,850) (15,280,778) (14,025,372)
Other income (expense):        
Foreign exchange gain (loss) 133,889 (406,486) 726,214 (773,500)
Interest expense (2,646,558) (971) (5,252,030) (971)
Investment income, net 127,902 161,258 295,100 273,479
Other, net (15,552)   (15,552)  
Loss before income taxes (10,096,028) (9,982,049) (19,527,046) (14,526,364)
Provision for income taxes        
Net loss $ (10,096,028) $ (9,982,049) $ (19,527,046) $ (14,526,364)
Net loss per common share - basic and diluted $ (0.73) $ (0.73) $ (1.40) $ (1.09)
Weighted average shares outstanding - basic and diluted 13,923,258 13,682,734 13,911,993 13,322,531
XML 15 R23.htm IDEA: XBRL DOCUMENT  v2.3.0.11
Commitments and Contingencies
6 Months Ended
Jun. 30, 2011
Commitments and Contingencies [Abstract]  
Commitments and Contingencies
Note 16. Commitments and Contingencies
At June 30, 2011, we had purchase order commitments of approximately $26.3 million related to product costs and property, plant and equipment purchases. Many of our materials and supplies require long lead times and as such purchase order commitments reflect materials that may be received up to one year from the date of order.
From time to time we may be involved in litigation or other contingencies arising in the ordinary course of business. Except as set forth below or in our 2010 Annual Report on Form 10-K, and based on the information presently available, management believes that there are no contingencies, claims or actions, pending or threatened, the ultimate resolution of which will have a material adverse effect on our financial position, liquidity or result of operations.
On February 24, 2010 we received a letter from two holders of Series A Preferred Stock in HeartWare, Inc., an indirect subsidiary of HeartWare International, Inc. These holders requested various financial and other information regarding HeartWare, Inc. for the purpose of determining the Company’s compliance with their rights as holders of Series A Preferred Stock, including whether a liquidation event has occurred since inception in 2003. HeartWare, Inc. issued Series A-1 and Series A-2 Preferred Stock to certain equity holders of Kriton Medical, Inc. when HeartWare, Inc. purchased substantially all of the assets of Kriton in July 2003. The Series A-1 and Series A-2 Preferred Stock do not have voting or dividend rights but entitle the holders thereof to receive, upon certain liquidation events of HeartWare, Inc. (but not the liquidation of or change of control of HeartWare International, Inc.), an amount equal to $10 per share of Series A-1 and $21 per share of Series A-2. The aggregate liquidation preference payment obligation totals approximately $15 million.
On June 27, 2011, HeartWare International, Inc. and HeartWare, Inc., along with HeartWare’s directors, certain officers and a significant stockholder, were named as defendants in a putative class action lawsuit filed in Massachusetts state court by two other Series A Preferred Stockholders on behalf of all holders of Series A Preferred Stock. The complaint alleges that the defendants breached their fiduciary and contractual obligations to Series A Preferred Stockholders by preventing them from receiving a payment of the liquidation preference in connection with certain corporate transactions, including a transaction in 2005 in which HeartWare, Inc. was acquired by HeartWare Limited, a subsidiary of HeartWare International, Inc. The plaintiffs seek monetary damages, interest, costs and limited equitable relief. We do not believe HeartWare International, Inc., HeartWare, Inc. or any of our directors, officers or stockholders have abrogated the rights, or in any way failed to satisfy obligations owed to, any of our stockholders, including holders of Series A Preferred Stock. We intend to vigorously defend the suit.
In accordance with ASC 450, Contingencies, we accrue loss contingencies including costs of settlement, damages and defense related to litigation to the extent they are probable and estimable. Otherwise, we expense these costs as incurred. If the estimate of a probable loss is a range and no amount within the range is more likely, we accrue the minimum amount of the range. As of June 30, 2011 we have not accrued any amounts related to the above litigation.
XML 16 R1.htm IDEA: XBRL DOCUMENT  v2.3.0.11
Document and Entity Information
6 Months Ended
Jun. 30, 2011
Jul. 27, 2011
Document and Entity Information [Abstract]    
Entity Registrant Name HeartWare International, Inc.  
Entity Central Index Key 0001389072  
Document Type 10-Q  
Document Period End Date Jun. 30, 2011
Amendment Flag false  
Document Fiscal Year Focus 2011  
Document Fiscal Period Focus Q2  
Current Fiscal Year End Date --12-31  
Entity Well-known Seasoned Issuer Yes  
Entity Voluntary Filers No  
Entity Current Reporting Status Yes  
Entity Filer Category Accelerated Filer  
Entity Common Stock, Shares Outstanding   13,925,984
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XML 18 R12.htm IDEA: XBRL DOCUMENT  v2.3.0.11
Foreign Exchange Instruments
6 Months Ended
Jun. 30, 2011
Foreign Exchange Instruments [Abstract]  
Foreign Exchange Instruments
Note 5. Foreign Exchange Instruments
During the quarter ended June 30, 2011, we entered into a foreign currency forward-exchange contract in an effort to minimize the risk of future fluctuations in the exchange rates between Australian dollars and Japanese Yen. The foreign currency forward-exchange contract was directly related to an asset purchase commitment by our Australian subsidiary. We do not utilize derivative financial instruments for speculative or trading purposes.
As of June 30, 2011, the forward contract to sell Australian dollars to Japanese Yen had a notional value of AU$858,000 and an exchange rate of one Australian dollar to 83.35 Japanese Yen. During the quarter ended June 30, 2011, the realized fair value of this forward exchange contract resulted in an expense of $16,000, which is included in other, net on the condensed consolidated statements of operations.
XML 19 R17.htm IDEA: XBRL DOCUMENT  v2.3.0.11
Accrued Expenses and Other Current Liabilities
6 Months Ended
Jun. 30, 2011
Accrued Expenses and Other Current Liabilities [Abstract]  
Accrued Expenses and Other Current Liabilities
Note 10. Accrued Expenses and Other Current Liabilities
Accrued expenses and other current liabilities consist of the following:
                 
    June 30,     December 31,  
    2011     2010  
Accrued payroll and other employee costs
  $ 3,345,268     $ 4,152,833  
Accrued material purchases
    2,245,440       255,679  
Accrued professional fees
    693,538       577,237  
Accrued research and development costs
    436,839       671,928  
Accrued VAT
    356,690       647,525  
Accrued interest payable on convertible senior notes
    209,635       209,635  
Other accrued expenses
    1,043,679       486,513  
 
           
 
  $ 8,331,089     $ 7,001,350  
 
           
Accrued payroll and other employee costs included estimated year-end employee bonuses of approximately $1.9 million and $3.1 million at June 30, 2011 and December 31, 2010, respectively.
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Basis of Presentation
6 Months Ended
Jun. 30, 2011
Basis of Presentation [Abstract]  
Basis of Presentation
Note 1. Basis of Presentation
HeartWare International, Inc., referred to in these notes collectively with its subsidiaries HeartWare Pty. Limited, HeartWare, Inc., HeartWare (UK) Limited and HeartWare GmbH as “we,” “our,” “HeartWare” or the “Company,” is a medical device company that develops and manufactures small implantable heart pumps, or ventricular assist devices, used in the treatment of advanced heart failure.
The accompanying unaudited interim condensed consolidated financial statements have been prepared pursuant to the rules and regulations of the Securities and Exchange Commission (“SEC”) for reporting of interim financial information. Pursuant to such rules and regulations, certain information and footnote disclosures normally included in financial statements prepared in accordance with accounting principles generally accepted in the United States have been condensed or omitted. Accordingly, these statements do not include all the disclosures normally required by accounting principles generally accepted in the United States for annual financial statements and should be read in conjunction with Management’s Discussion and Analysis of Financial Condition and Results of Operations contained in this report and the audited financial statements and notes thereto for the year ended December 31, 2010 included in our Annual Report on Form 10-K. The accompanying condensed consolidated balance sheet as of December 31, 2010 has been derived from our audited financial statements. The condensed consolidated statements of operations for the three and six months ended June 30, 2011 and cash flows for the six months ended June 30, 2011 are not necessarily indicative of the results to be expected for any future period or for the year ending December 31, 2011.
In the opinion of management, the accompanying unaudited interim condensed consolidated financial statements contain all adjustments (consisting of only normally recurring adjustments) necessary to present fairly the financial position and results of operations as of the dates and for the periods presented.

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Inventories, Net
6 Months Ended
Jun. 30, 2011
Inventories, Net [Abstract]  
Inventories, Net
Note 7. Inventories, Net
Components of inventories, net are as follows:
                 
    June 30,     December 31,  
    2011     2010  
 
Raw material
  $ 5,194,259     $ 4,279,170  
Work-in-process
    4,181,495       2,708,840  
Finished goods
    13,146,602       8,088,580  
 
           
 
  $ 22,522,356     $ 15,076,590  
 
           
Finished goods inventories includes inventory held on consignment at customer sites of $5.4 million and $4.7 million, at June 30, 2011 and December 31, 2010, respectively.
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Stockholders' Equity
6 Months Ended
Jun. 30, 2011
Stockholders' Equity [Abstract]  
Stockholders' Equity
Note 12. Stockholders’ Equity
In February 2010, we completed a public offering of approximately 1.77 million shares of our common stock, including the underwriter’s exercise of their overallotment to purchase 230,595 shares, at an offering price of $35.50 per share for aggregate gross proceeds of approximately $62.8 million. The underwriters for the transaction received a fee of 6% of the gross proceeds. After fees and related expenses, net proceeds from the offering were approximately $58.5 million.
The offering was completed pursuant to a prospectus supplement, dated January 27, 2010, to a shelf registration statement on Form S-3 that was previously filed with the SEC and which was declared effective on January 20, 2010. This shelf registration statement allows us to offer and sell from time to time, in one or more series or issuances and on terms that we will determine at the time of the offering, any combination of the securities described in the prospectus, up to an aggregate amount of $100 million.
In the six months ended June 30, 2011, we issued an aggregate of 17,606 shares of our common stock upon the exercise of stock options and an aggregate of 29,692 shares of our common stock upon the vesting of restricted stock units.
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Property, Plant and Equipment, Net
6 Months Ended
Jun. 30, 2011
Property, Plant and Equipment, Net [Abstract]  
Property, Plant and Equipment, Net
Note 8. Property, Plant and Equipment, Net
Property, plant and equipment, net consists of the following:
                         
    Estimated     June 30,     December 31,  
    Useful Lives     2011     2010  
Machinery and equipment
    1.5 to 7 years     $ 11,225,797     $ 8,966,747  
Leasehold improvements
    3 to 7 years       1,835,365       282,483  
Office equipment, furniture and fixtures
    5 to 7 years       913,516       450,849  
Purchased software
    5 to 7 years       2,104,057       1,741,132  
 
                   
 
            16,078,735       11,441,211  
Less: accumulated depreciation
            (4,948,383 )     (3,957,189 )
 
                   
 
          $ 11,130,352     $ 7,484,022  
 
                   
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Fair Value Measurements
6 Months Ended
Jun. 30, 2011
Fair Value Measurements [Abstract]  
Fair Value Measurements
Note 6. Fair Value Measurements
FASB ASC 820 — Fair Value Measurements and Disclosures, defines fair value as the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement date. FASB ASC 820 requires disclosures about the fair value of all financial instruments, whether or not recognized, for financial statement purposes. Disclosures about the fair value of financial instruments are based on pertinent information available to us as of the reporting dates. Accordingly, the estimates presented in these condensed consolidated financial statements are not necessarily indicative of the amounts that could be realized on disposition of the financial instruments.
FASB ASC 820 specifies a hierarchy of valuation techniques based on whether the inputs to those valuation techniques are observable or unobservable. Observable inputs reflect market data obtained from independent sources, while unobservable inputs reflect market assumptions. The hierarchy gives the highest priority to unadjusted quoted prices in active markets for identical assets or liabilities (Level 1 measurement) and the lowest priority to unobservable inputs (Level 3 measurement).
The three levels of the fair value hierarchy are as follows:
Level 1 — Quoted prices for identical instruments in active markets.
Level 2 — Quoted prices for similar instruments in active markets; quoted prices for identical or similar instruments in markets that are not active; and model-derived valuations whose inputs are observable or whose significant value drivers are observable.
Level 3 — Instruments with primarily unobservable value drivers.
The following table represents the fair value of our financial assets and financial liabilities measured at fair value on a recurring basis and which level was used in the fair value hierarchy.
                                         
    At June 30, 2011  
    Carrying     Fair     Fair Value Measurements at the Reporting Date Using  
    Value     Value     Level 1     Level 2     Level 3  
Assets
                                       
Short-term investments
  $ 79,998,132     $ 79,998,132     $     $ 79,998,132     $  
 
                                       
Liabilities
                                       
Foreign exchange instrument
    15,547       15,547             15,547        
Convertible senior notes
    91,518,710 (1)     151,117,188             151,117,188        
                                         
    At December 31, 2010  
    Carrying     Fair     Fair Value Measurements at the Reporting Date Using  
    Value     Value     Level 1     Level 2     Level 3  
Assets
                                       
Short-term investments
  $ 21,330,110     $ 21,330,110     $       21,330,110     $  
Long-term investments
    4,005,659       4,005,659             4,005,659        
 
                                       
Liabilities
                                       
Convertible senior notes
    88,921,557 (1)     160,693,813             160,693,813        
(1)   The carrying amount of our convertible senior notes is net of unamortized discount. See Note 11, “Debt” for more information.
The fair value of our investments was determined using quoted prices for the instruments in markets that are not active. The fair value of our foreign exchange instrument was determined using observable market data such as pricing for similar instruments or recently executed transactions. The fair value of our convertible senior notes was determined using observable market data (including trade data) and is presented for disclosure purposes only.
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Condensed Consolidated Statement of Stockholders' Equity (Unaudited) (USD $)
Total
Common Shares Shares Issued
Additional Paid-In Capital
Accumulated Deficit
Accumulated Other Comprehensive Loss
Beginning balance at Dec. 31, 2010 $ 167,764,354 $ 13,879 $ 302,533,344 $ (127,268,545) $ (7,514,324)
Beginning balance, shares at Dec. 31, 2010   13,878,686      
Issuance of common stock pursuant to share-based awards, shares   47,298      
Issuance of common stock pursuant to share-based awards 599,614 47 599,567    
Share-based compensation 6,436,813   6,436,813    
Net loss (19,527,046)     (19,527,046)  
Other comprehensive loss:          
Foreign currency translation adjustments 91,445       91,445
Unrealized loss on investments (25,307)       (25,307)
Ending balance at Jun. 30, 2011 $ 155,339,873 $ 13,926 $ 309,569,724 $ (146,795,591) $ (7,448,186)
Ending balance, shares at Jun. 30, 2011   13,925,984      
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Liquidity
6 Months Ended
Jun. 30, 2011
Liquidity [Abstract]  
Liquidity
Note 2. Liquidity
At June 30, 2011, we had approximately $198.8 million of cash, cash equivalents and investments. The accompanying condensed consolidated financial statements have been prepared in conformity with accounting principles generally accepted in the United States, which contemplates continuation of the Company as a going concern. We have sustained substantial losses from operations since our inception, and such losses have continued through June 30, 2011. At June 30, 2011, we had an accumulated deficit of approximately $146.8 million.
We have financed our operations primarily through the issuance of shares of our common stock and the issuance of convertible notes. Most recently, in December 2010, we consummated the issuance and sale of $143.75 million aggregate principal amount of convertible notes. The convertible notes are the senior unsecured obligations of the Company. The convertible notes bear interest at a rate of 3.5% per annum, payable semi-annually in arrears on June 15 and December 15 of each year, beginning on June 15, 2011. The convertible notes will mature on December 15, 2017, unless earlier repurchased or converted. The convertible notes will be convertible at an initial conversion rate of 10 shares of common stock per $1,000 principal amount of convertible notes, which corresponds to an initial conversion price of $100.00 per share of common stock.
For the remainder of 2011, our cash, cash equivalents and investments are expected to primarily be used to fund our ongoing operations including expanding our sales and marketing capabilities on a global basis, continuing our ENDURANCE trial for destination therapy, enrolling additional patients in our ADVANCE trial under a Continued Access Protocol (“CAP”), continued product development, regulatory and other compliance functions, including costs related to testing and submission of our PMA application, as well as for general working capital. We believe our cash, cash equivalent and investment balances are sufficient to support our planned operations through 2012.
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Significant Accounting Policies
6 Months Ended
Jun. 30, 2011
Significant Accounting Policies [Abstract]  
Significant Accounting Policies
Note 3. Significant Accounting Policies
Principles of Consolidation
The condensed consolidated financial statements include the accounts of HeartWare International, Inc., and its subsidiaries described in Note 1. All inter-company balances and transactions have been eliminated in consolidation.
Accounting Estimates
The preparation of consolidated financial statements in conformity with accounting principles generally accepted in the United States (“US GAAP”) requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities, the disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting periods. Actual results could differ from those estimates.
Cash and Cash Equivalents
Cash and cash equivalents are recorded in the condensed consolidated balance sheets at cost, which approximates fair value. All highly liquid investments with an original maturity of three months or less at the date of purchase are considered to be cash equivalents.
Investments
Our investments classified as available-for-sale are stated at fair value with unrealized gains and losses reported in accumulated other comprehensive loss within stockholders’ equity. We classify our available-for-sale investments as short-term if their remaining time to maturity at purchase is beyond three months. Investments with maturities beyond one year may be classified as short-term based on their highly liquid nature and because such marketable securities represent the investment of cash that is available for current operations. Interest on investments classified as available-for-sale is included in investment income, net. Premiums paid on our short-term investments are amortized over the remaining term of the investment and such amortization is included in investment income, net.
Receivables
Accounts receivable consists of amounts due from the sale of our HeartWare® Ventricular Assist System (the “HeartWare System”) to our customers, which include hospitals, health research institutions and medical device distributors. Our receivables are geographically dispersed, with a significant portion from customers located in Europe and other foreign countries. As of June 30, 2011 and December 31, 2010, one customer had an accounts receivable balance representing approximately 11% and 13%, respectively, of our total accounts receivable.
We maintain allowances for doubtful accounts for estimated losses that may result from an inability to collect payments owed to us for product sales. We regularly review the allowance by considering factors such as historical experience, the age of the accounts receivable balances and current economic conditions that may affect a customer’s ability to pay.
The following table summarizes the change in our allowance for doubtful accounts for the six months ended June 30, 2011 and 2010:
                 
    Six months ended  
    June 30,  
    2011     2010  
Beginning balance
  $ 600,000     $  
Additions (bad debt expense)
    300,000       285,000  
Deductions (charge-offs)
           
 
           
Ending balance
  $ 900,000     $ 285,000  
 
           
As of June 30, 2011 and December 31, 2010, we did not have an allowance for returns.
Inventories, net
Inventories are stated at the lower of cost or market. Cost is determined using a first-in, first-out, or FIFO, method. Work-in-process and finished goods include direct and indirect labor and manufacturing overhead. Finished goods include product which is ready-for-use and which is held by us or by our customers on a consignment basis.
We review our inventory for excess or obsolete inventory and write-down obsolete or otherwise unmarketable inventory to its estimated net realizable value. Obsolescence may occur due to product expiring or product improvements rendering previous versions obsolete. In May 2011, we began shipping a sintered version of the HeartWare System on a global basis. Sintering is commonly used in medical devices to facilitate tissue adhesion. The extent to which this product enhancement will cause obsolescence of existing non-sintered inventory is difficult to determine because the rate of product adoption of sintered product is dependent on individual customer acceptance, implantation rates and approval timeframes of Institutional Review Boards at U.S. sites. As of June 30, 2011, we had $3.5 million of non-sintered inventory on hand and this product continues to be implanted at customer sites. However, a write-down of all or a portion of this inventory as obsolete could have a material impact on our results of operations.
Deferred Financing Costs
Costs incurred in connection with the issuance of our convertible senior notes in December 2010 have been allocated between the liability component and the equity component as further discussed in Note 11. The liability component of the issuance costs incurred was capitalized and is included in deferred financing costs, net on the condensed consolidated balance sheets. These costs are being amortized using the effective interest method through December 15, 2017, the maturity date of the notes, and such amortization expense is reflected in interest expense on our condensed consolidated statements of operations. The amount of amortization for the three and six months ended June 30, 2011 was approximately $71,000 and $139,000, respectively.
Product Warranty
Certain patient accessories sold with the HeartWare System are covered by a limited warranty ranging from one to two years. Estimated contractual warranty obligations are recorded as an expense when the related revenue is recognized and are included in cost of revenues on the condensed consolidated statements of operations. Factors that affect the estimated warranty liability include the number of units sold, historical and anticipated rates of warranty claims, cost per claim, and vendor supported warranty programs. We periodically assess the adequacy of our recorded warranty liabilities and adjust the amounts as necessary.
The amount of the liability recorded is equal to the estimated costs to repair or otherwise satisfy claims made by customers. Accrued warranty expense is included as a component of accrued expenses and other current liabilities on the condensed consolidated balance sheets.
The costs to repair or replace products associated with product recalls and voluntary service campaigns are recorded when they are determined to be probable and reasonably estimable as a cost of revenues and are not included in the product warranty liability. No such costs were incurred in the six months ended June 30, 2011 and approximately $411,000 was incurred in the six months ended June 30, 2010.
The following table summarizes the change in our warranty liability for the six months ended June 30, 2011 and 2010:
                 
    Six months ended  
    June 30,  
    2011     2010  
Beginning balance
  $ 290,891     $ 99,169  
Accrual for (reversal of) warranty expense
    (20,491 )     97,362  
Warranty costs incurred during the period
    (28,295 )     (47,363 )
 
           
Ending balance
  $ 242,105     $ 149,168  
 
           
Fair Value Measurements
The carrying amounts reported in the condensed consolidated balance sheets for cash and cash equivalents, accounts receivable, accounts payable and accrued expenses and other current liabilities approximate their fair value based on the short-term maturity of these instruments. Investments are considered available-for-sale as of June 30, 2011 and December 31, 2010 and are carried at fair value. See Note 6, “Fair Value Measurements” and Note 10, “Debt” for more information.
Vendor Concentration
For the three and six months ended June 30, 2011, we purchased approximately 55% of our inventory components and supplies from two vendors. For the three and six months ended June 30, 2010, we purchased approximately 62% and 51%, respectively, of our inventory components and supplies from the same two vendors. In addition, one of these vendors supplies consulting services and material used in research and development activities. As of June 30, 2011 and 2010, the amounts due to these vendors totaled approximately $788,000 and $1.1 million, respectively.
Concentration of Credit Risk and other Risks and Uncertainties
Financial instruments that potentially expose us to concentrations of credit risk consist primarily of cash and cash equivalents, investments and trade accounts receivable. Cash and cash equivalents are primarily on deposit with financial institutions in the United States and these deposits generally exceed the amount of insurance provided by the Federal Deposit Insurance Corporation (the “FDIC”). The Company has not experienced any historical losses on its deposits of cash and cash equivalents. Our investments consist of investment grade rated corporate and government agency debt.
Concentration of credit risk with respect to our trade accounts receivable from our customers is primarily limited to hospitals, health research institutions and medical device distributors. Credit is extended to our customers, based on an evaluation of a customer’s financial condition and collateral is not required. To date, we have not experienced any credit losses, but have established an allowance for doubtful accounts of $900,000 at June 30, 2011.
We are subject to certain risks and uncertainties including, but not limited to, our ability to achieve profitability, to generate cash flow sufficient to satisfy our indebtedness, to run clinical trials in order to receive and maintain FDA and foreign regulatory approvals for our products, the ability to achieve widespread acceptance of our product, our ability to manufacture our products in a sufficient volume and at a reasonable cost, the ability to protect our proprietary technologies and develop new products, the risks associated with operating in foreign countries, and general competitive and economic conditions. Changes in any of the preceding areas could have a material adverse effect on our business, results of operations or financial position.
New Accounting Standards
In May 2011, the Financial Accounting Standards Board (FASB) issued Accounting Standards Update (ASU) No. 2011-04, Fair Value Measurement (Topic 820): Amendments to Achieve Common Fair Value Measurement and Disclosure Requirements in U.S. GAAP and IFRSs. ASU No. 2011-04 clarifies some existing concepts, eliminates wording differences between U.S. GAAP and International Financial Reporting Standards (“IFRS”), and in some limited cases, changes some principles to achieve convergence between U.S. GAAP and IFRS. ASU No. 2011-04 results in a consistent definition of fair value and common requirements for measurement of and disclosure about fair value between U.S. GAAP and IFRS. ASU No. 2011-04 also expands the disclosures for fair value measurements that are estimated using significant unobservable (Level 3) inputs. The provisions of ASU No. 2011-04 will become effective for us on January 1, 2012 and are to be applied prospectively. We do not expect the adoption of the provisions of ASU No. 2011-04 to have a material effect on our consolidated financial position, results of operations or cash flows and we do not expect to materially modify or expand our financial statement footnote disclosures.
In June 2011, the FASB issued ASU No. 2011-05, Comprehensive Income (Topic 220): Presentation of Comprehensive Income. ASU No. 2011-05 requires an entity to present the total of comprehensive income, the components of net income, and the components of other comprehensive income either in a single continuous statement of comprehensive income, or in two separate but consecutive statements. ASU No. 2011-05 eliminates the option to present components of other comprehensive income as part of the statement of stockholders’ equity. The presentation requirements will become effective for us on January 1, 2012. As ASU No. 2011-05 applies to financial statement presentation matters, the adoption of ASU No. 2011-05 will not affect our consolidated financial position, results of operations or cash flows and we believe our current presentation of comprehensive income complies with the new presentation requirements.
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Debt
6 Months Ended
Jun. 30, 2011
Debt [Abstract]  
Debt
Note 11. Debt
Convertible Senior Notes
On December 15, 2010, we completed the sale of 3.5% convertible senior notes due 2017 (the “Convertible Notes”) for an aggregate principal amount of $143.75 million pursuant to the terms of an Indenture dated December 15, 2010. The Convertible Notes are the senior unsecured obligations of the Company. The Convertible Notes bear interest at a rate of 3.5% per annum, payable semi-annually in arrears on June 15 and December 15 of each year, beginning on June 15, 2011. The Convertible Notes will mature on December 15, 2017, unless earlier repurchased by us or converted.
The Convertible Notes will be convertible at an initial conversion rate of 10 shares of our common stock per $1,000 principal amount of Convertible Notes, which corresponds to an initial conversion price of $100.00 per share of our common stock representing a conversion premium of approximately 23% based on the closing price of $81.31 per share of our common stock on December 9, 2010, the day the notes were priced. The conversion rate is subject to adjustment from time to time upon the occurrence of certain events.
Prior to June 15, 2017, holders may convert their Convertible Notes at their option only upon satisfaction of one or more conditions relating to the sale price of our common stock, the trading price per $1,000 principal amount of Convertible Notes or specified corporate events. On or after June 15, 2017, until the close of business of the business day immediately preceding the date the Convertible Notes mature, holders may convert their Convertible Notes at any time, regardless of whether any of the foregoing conditions have been met. As of the date of this report, none of the events that would allow holders to convert their Convertible Notes have occurred. Upon conversion, we will pay or deliver, as the case may be, cash, shares of our common stock or a combination thereof, at our election.
In accordance with ASC 470-20, Debt, which applies to certain convertible debt instruments that may be settled in cash or other assets, or partially in cash, upon conversion, we recorded the long-term debt and equity components on our Convertible Notes separately on the issuance date. The amount recorded for long-term debt was determined by measuring the fair value of a similar liability that does not have an associated equity component. The measurement of fair value required the Company to make estimates and assumptions to determine the present value of the cash flows of the Convertible Notes, absent the conversion feature. This treatment increased interest expense associated with our Convertible Notes by adding a non-cash component to amortize a debt discount calculated based on the difference between the 3.5% cash coupon rate and the effective interest rate on debt borrowing of approximately 12.5%. The discount is being amortized to interest expense through the December 15, 2017 maturity date of the Convertible Notes using the effective interest method and is included in interest expense on the condensed consolidated statements of operations. Additionally, we allocated the costs related to issuance of the Convertible Notes on the same percentage as the long-term debt and equity components, such that a portion of the costs is allocated to the long-term debt component and the equity component included in additional paid-in capital. The portion of the costs allocated to the long-term debt component is presented as deferred financing costs, net on our condensed consolidated balance sheets. These deferred financing costs are also being amortized to interest expense through the December 15, 2017 maturity date of the Convertible Notes using the effective interest method and such amortization is included in interest expense on the condensed consolidated statements of operations
The Convertible Notes and the equity component, which is recorded in additional paid-in-capital, consisted of the following:
                 
    June 30,     December 31,  
    2011     2010  
Principal amount
  $ 143,750,000     $ 143,750,000  
Unamortized discount
    (52,231,290 )     (54,828,443 )
 
           
Net carrying amount
  $ 91,518,710     $ 88,921,557  
 
           
Equity component
  $ 55,037,913     $ 55,037,913  
 
           
Based on the initial conversion rate of 10 shares of our common stock per $1,000 principal amount of Convertible Notes, which corresponds to an initial conversion price of $100.00 per share of our common stock, the number of shares issuable upon conversion of the Convertible Notes is 1,437,500. The value of these shares, based on the closing price of our common stock on June 30, 2011 of $74.08, was approximately $106.5 million. The fair value of our Convertible Notes as presented in Note 6 was $151.1 million and $160.7 million at June 30, 2011 and December 31, 2010, respectively.
Interest expense related to the Convertible Notes consisted of interest due on the principal amount, amortization of the discount and amortization of the portion of the deferred financing costs allocated to the long-term debt component. For the three and six months ended June 30, 2011, interest expense related to the Convertible Notes was as follows:
                 
    Three Months     Six Months  
    Ended     Ended  
    June 30, 2011     June 30, 2011  
Stated amount at 3.5% coupon rate
  $ 1,257,812     $ 2,515,625  
Amortization of discount
    1,318,074       2,597,153  
Amortization of deferred financing costs
    70,672       139,252  
 
           
 
  $ 2,646,558     $ 5,252,030  
 
           
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Investments
6 Months Ended
Jun. 30, 2011
Investments [Abstract]  
Investments
Note 4. Investments
We have cash investment policies that limit investments to investment grade securities. At June 30, 2011 and December 31, 2010, all of our investments were classified as available-for-sale and carried at fair value. Our investments in corporate debt are guaranteed by the FDIC or foreign governments. At June 30, 2011, all of our investments had maturity dates of less than twenty-four months.
The amortized cost and fair value of our investments, with gross unrealized gains and losses, were as follows:
At June 30, 2011
                                 
            Gross     Gross        
    Amortized     Unrealized     Unrealized     Aggregate  
    Cost Basis     Gains     Losses     Fair Value  
 
Short-term investments:
                               
U.S. government agency debt
  $ 49,806,325     $ 6,982     $ (22,236 )   $ 49,791,071  
Corporate debt
    15,182,732       24,329             15,207,061  
Certificates of deposit
    15,000,000                   15,000,000  
 
                       
 
                               
Total short-term investments
  $ 79,989,057     $ 31,311     $ (22,236 )   $ 79,998,132  
 
                       
     At December 31, 2010
                                 
            Gross     Gross        
    Amortized     Unrealized     Unrealized     Aggregate  
    Cost Basis     Gains     Losses     Fair Value  
 
Short-term investments:
                               
Corporate debt
  $ 21,294,673     $ 35,437     $     $ 21,330,110  
 
                       
 
                               
Total short-term investments
  $ 21,294,673     $ 35,437     $     $ 21,330,110  
 
                       
 
                               
Long-term investments:
                               
U.S. government agency debt
  $ 4,006,714     $     $ (1,055 )   $ 4,005,659  
 
                       
 
                               
Total long-term investments
  $ 4,006,714     $     $ (1,055 )   $ 4,005,659  
 
                       
For the three and six months ended June 30, 2011 and 2010 we did not have any realized gains or losses on our investments.
XML 32 R21.htm IDEA: XBRL DOCUMENT  v2.3.0.11
Net Loss Per Common Share
6 Months Ended
Jun. 30, 2011
Net Loss Per Common Share [Abstract]  
Net Loss Per Common Share
Note 14. Net Loss Per Common Share
Basic net loss per common share is computed by dividing net loss for the period by the weighted-average number of common shares outstanding during the period. Diluted net loss per common share adjusts basic net loss per common share for the dilutive effects of convertible securities, options and other potentially dilutive instruments only in the periods in which such effect is dilutive. Due to our net loss for all periods presented, all potentially dilutive instruments were excluded because their inclusion would have been anti-dilutive. The following instruments have been excluded from the calculation of diluted net loss per common share, as their effect would be anti-dilutive.
                 
    Three and Six Months Ended  
    June 30,  
    2011     2010  
Common shares issuable upon:
               
Conversion of convertible senior notes
    1,767,923        
Exercise of share-based awards
    953,237       915,201  
XML 33 R5.htm IDEA: XBRL DOCUMENT  v2.3.0.11
Condensed Consolidated Statements of Comprehensive Loss (Unaudited) (USD $)
3 Months Ended 6 Months Ended
Jun. 30, 2011
Jun. 30, 2010
Jun. 30, 2011
Jun. 30, 2010
Condensed Consolidated Statements of Comprehensive Loss [Abstract]        
Net loss $ (10,096,028) $ (9,982,049) $ (19,527,046) $ (14,526,364)
Foreign currency translation adjustments 64,938 (139,455) 91,445 (62,738)
Unrealized gain (loss) on investments 7,751 (21,332) (25,307) (45,124)
Comprehensive loss $ (10,023,339) $ (10,142,836) $ (19,460,908) $ (14,634,226)
XML 34 R22.htm IDEA: XBRL DOCUMENT  v2.3.0.11
Business Segment, Geographic Areas and Major Customers
6 Months Ended
Jun. 30, 2011
Business Segment, Geographic Areas and Major Customers [Abstract]  
Business Segment, Geographic Areas and Major Customers
Note 15. Business Segment, Geographic Areas and Major Customers
For financial reporting purposes, we have one reportable segment which designs, manufactures and markets medical devices for the treatment of advanced heart failure. Generally, products are sold to customers located in the United States through our clinical trials, as commercial products to customers in Europe and under special access in other countries. Product sales attributed to a country or region are based on the location of the customer to whom the products are sold. Long-lived assets are primarily held in the United States.
Product sales by geographic location are as follows:
                                 
    Three Months Ended     Six Months Ended  
    June 30,     June 30,  
(in thousands)   2011     2010     2011     2010  
Domestic
  $ 6,291     $ 1,865     $ 12,189     $ 4,547  
Germany
    8,214       5,283       13,712       10,839  
International, excluding Germany
    5,884       2,609       12,463       5,074  
 
                       
 
  $ 20,389     $ 9,757     $ 38,364     $ 20,460  
 
                       
For the three and six months ended June 30, 2011, one customer accounted for approximately 11% and 10%, respectively, of product sales in the aggregate. For the three and six months ended June 30, 2010, two customers exceeded 10% of product sales individually and accounted for approximately 30% and 29%, respectively, of product sales in the aggregate. As the majority of our revenue is generated outside of the U.S., we are dependent on favorable economic and regulatory environments for our products in Europe and other countries outside of the U.S.
The percentage of our revenue generated in the U.S. was lower in 2010 compared to 2011 due to the completion of enrollment in our ADVANCE trial in the U.S. in February 2010. While the FDA approved an Investigational Device Exemption Supplement that allowed us to enroll additional patients in our ADVANCE trial under a Continued Access Protocol, we did not recommence enrollment in our ADVANCE trial until the second quarter of 2010 while we awaited approval. Also contributing to the increase in the percentage of our revenue generated in the U.S. in 2011 was continued enrollment in our ENDURANCE destination therapy clinical trial in the U.S., which commenced in August 2010.
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Subsequent Events
6 Months Ended
Jun. 30, 2011
Subsequent Events [Abstract]  
Subsequent Events
Note 17. Subsequent Events
We have evaluated events and transactions that occurred subsequent to June 30, 2011 through the date the financial statements were issued, for potential recognition or disclosure in the accompanying condensed consolidated financial statements.
We did not identify any events or transactions that should be recognized or disclosed in the accompanying condensed consolidated financial statements.
XML 36 R7.htm IDEA: XBRL DOCUMENT  v2.3.0.11
Condensed Consolidated Statements of Cash Flows (Unaudited) (USD $)
6 Months Ended
Jun. 30, 2011
Jun. 30, 2010
CASH FLOWS FROM OPERATING ACTIVITIES    
Net loss $ (19,527,046) $ (14,526,364)
Adjustments to reconcile net loss to net cash used in operating activities:    
Depreciation of property, plant and equipment 1,019,609 580,536
Amortization of intangible assets 63,887 47,862
Share-based compensation expense 6,436,813 5,998,962
Amortization of premium on investments 440,507 167,056
Amortization of discount on convertible senior notes 2,597,153  
Amortization of deferred financing costs 139,252  
Other 340,100 284,998
Change in operating assets and liabilities:    
Accounts receivable 3,526,642 3,528,615
Inventories, net (7,547,061) (6,757,485)
Prepaid expenses and other current assets (2,247,717) (389,974)
Accounts payable (554,869) 356,854
Accrued expenses and other current liabilities 1,309,423 1,430,473
Net cash used in operating activities (14,003,307) (9,278,467)
CASH FLOWS FROM INVESTING ACTIVITIES    
Purchases of investments (80,128,177) (16,644,600)
Maturities of investments 25,000,000  
Additions to property, plant and equipment (4,667,787) (2,497,481)
Additions to patents (253,940) (283,410)
Proceeds from disposition of assets 98,225  
Net cash used in investing activities (59,951,679) (19,425,491)
CASH FLOWS FROM FINANCING ACTIVITIES    
Proceeds from issuance of common stock   62,760,450
Payment of common stock issuance costs (600) (4,359,934)
Proceeds from exercise of stock options 599,614 2,804,101
Net cash provided by financing activities 599,014 61,204,617
Effect of exchange rate changes on cash and cash equivalents 51,334 (9,402)
(DECREASE) INCREASE IN CASH AND CASH EQUIVALENTS (73,304,638) 32,491,257
CASH AND CASH EQUIVALENTS - BEGINNING OF PERIOD 192,148,312 50,834,714
CASH AND CASH EQUIVALENTS - END OF PERIOD $ 118,843,674 $ 83,325,971
XML 37 R16.htm IDEA: XBRL DOCUMENT  v2.3.0.11
Other Intangible Assets, Net
6 Months Ended
Jun. 30, 2011
Other Intangible Assets, Net [Abstract]  
Other Intangible Assets, Net
Note 9. Other Intangible Assets, Net
The gross carrying amount of intangible assets and the related accumulated amortization for intangible assets subject to amortization are as follows:
                                         
            June 30, 2011     December 31, 2010  
    Weighted Average Life     Gross Carrying     Accumulated     Gross Carrying     Accumulated  
Amortizable Intangible Assets   (Years)     Amount     Amortization     Amount     Amortization  
Patents
    15     $ 2,115,624     $ (330,115 )   $ 1,861,684     $ (266,228 )
Amortization expense for the three months ended June 30, 2011 and 2010 was approximately $33,000 and $25,000, respectively. Amortization expense for the six months ended June 30, 2011 and 2010 was approximately $64,000 and $48,000, respectively.
XML 38 R20.htm IDEA: XBRL DOCUMENT  v2.3.0.11
Share-Based Compensation
6 Months Ended
Jun. 30, 2011
Share-Based Compensation [Abstract]  
Share-Based Compensation
Note 13. Share-Based Compensation
We recognize share-based compensation expense for the portion of awards that are ultimately expected to vest using an accelerated accrual method over the vesting period from the date of grant. We estimate forfeitures at the time of grant. We have applied a forfeiture rate of approximately 12.5% to all unvested share-based awards as of June 30, 2011, which represents the portion that we expect will be forfeited over the vesting period. We reevaluate this estimated rate periodically and adjust the forfeiture rate as necessary. Vesting of share-based awards issued with performance-based vesting criteria must be “probable” before we begin recording share-based compensation expense. At each reporting period, we review the likelihood that these awards will vest and if the vesting is deemed probable, we begin to recognize compensation expense at that time. If ultimately performance goals are not met, for any awards where vesting was previously deemed probable, previously recognized compensation cost will be reversed.
We allocate share-based compensation expense to cost of revenues, selling, general and administrative expense and research and development expense based on the award holders’ employment function. For the three and six months ended June 30, 2011 and 2010, we recorded share-based compensation expense as follows:
                                 
    Three Months Ended     Six Months Ended  
    June 30,     June 30,  
    2011     2010     2011     2010  
Cost of revenues
  $ 533,644     $ 207,270     $ 1,118,862     $ 475,920  
Selling, general and administrative
    2,209,086       3,577,919       3,653,435       4,479,977  
Research and development
    758,703       487,306       1,664,516       1,043,065  
 
                       
 
  $ 3,501,433     $ 4,272,495     $ 6,436,813     $ 5,998,962  
 
                       
No deferred tax benefits were attributed to our share-based compensation expense recorded in the accompanying condensed consolidated financial statements because we are in a net operating loss position and a full valuation allowance is maintained for all net deferred tax assets. We receive a tax deduction for certain stock option exercises during the period the options are exercised, and for the vesting of restricted stock units during the period the restricted stock units vest. For stock options, the amount of the tax deduction is generally for the excess of the fair market value of our shares of common stock over the exercise price of the stock options at the date of exercise. For restricted stock units, the amount of the tax deduction is generally for the fair market value of our shares of common stock at the vesting date. Excess tax benefits are not included in the accompanying condensed consolidated financial statements because we are in a net operating loss position and a full valuation allowance is maintained for all net deferred tax assets.
Equity Plans
We have issued share-based awards to employees, non-executive directors and outside consultants through various approved plans and outside of any formal plan. New shares are issued upon the exercise of share-based awards.
On August 5, 2008, we adopted the HeartWare International, Inc. 2008 Stock Incentive Plan (“2008 SIP”). The 2008 SIP allows for the issuance of share-based awards to employees, directors and consultants. We have issued options and restricted stock units (“RSU’s”) to employees and directors under the 2008 SIP. The plan allows for the issuance of share-based awards representing up to 13% of the prior fiscal year’s weighted average shares outstanding, less share-based awards outstanding under our other equity plans. At June 30, 2011, there were approximately 619,000 shares available for future awards under the 2008 SIP.
Stock Options
Each option allows the holder to subscribe for and be issued one share of our common stock at a specified price, which is generally the quoted market price of our common stock on the date the option is issued. Options generally vest on a pro-rata basis on each anniversary of the issuance date within four years of the date the option is issued. Options may be exercised after they have vested and prior to the specified expiry date provided applicable exercise conditions are met, if any. The expiry date can be for periods of up to ten years from the date the option is issued.
In 2007 and 2008, we granted options with performance-based vesting criteria. These performance-based options vest in four equal tranches contingent upon the achievement of pre-determined corporate milestones related primarily to the development of our products and the achievement of certain prescribed clinical and regulatory objectives. Any performance-based options that have not vested after five years from the date of grant automatically expire.
The fair value of each option is estimated on the date of grant using the Black-Scholes option pricing model using the assumptions established at that time. The following table includes the assumptions used for options issued in the three and six months ended June 30, 2011 and 2010.
                                 
    Three Months Ended     Six Months Ended  
    June 30,     June 30,  
    2011     2010     2011     2010  
Dividend yield
    0 %     0 %     0 %     0 %
Expected volatility
    58.24 %     60.53 %     58.31 %     61.05 %
Risk-free interest rate
    2.10 %     2.63 %     2.16 %     2.81 %
Estimated holding period (years)
    6.25       6.25       6.25       6.25  
Information related to options granted under all of our plans at June 30, 2011 and activity in the six months then ended is as follows (certain amounts in US$ were converted from AU$ at the then period-end spot rate):
                                 
                    Weighted        
            Weighted     Average        
            Average     Remaining        
            Exercise     Contractual Life     Aggregate  
    Shares     Price     (Years)     Intrinsic Value  
Outstanding at December 31, 2010
    404,366     $ 32.87                  
Granted
    13,750       78.47                  
Exercised
    (17,606 )     34.06                  
Forfeited
    (8,991 )     37.51                  
Expired
                           
 
                             
Outstanding at June 30, 2011
    391,519     $ 35.37       6.31     $ 15,154,284  
 
                             
Exercisable at June 30, 2011
    246,960     $ 36.10       5.49     $ 9,379,109  
 
                             
The aggregate intrinsic values at June 30, 2011 noted in the table above represent the closing price of our common stock traded on NASDAQ, less the weighted average exercise price at period end multiplied by the number of options outstanding or exercisable.
At June 30, 2011, 34,283 of the 144,559 options outstanding that are not yet exercisable are subject to performance-based vesting criteria as described above.
The weighted average grant date fair value per share of options issued in the six months ended June 30, 2011 and 2010 was $44.36 and $27.08 per share, respectively.
The total intrinsic value of options exercised in the six months ended June 30, 2011 was approximately $971,000. Cash received from options exercised in the six months ended June 30, 2011 was approximately $600,000. The total intrinsic value of options exercised in the six months ended June 30, 2010 was approximately $2.8 million. Cash received from options exercised in the six months ended June 30, 2010 was approximately $2.8 million.
At June 30, 2011, there was approximately $1.4 million of unrecognized compensation cost related to non-vested option awards, including performance-based options not yet deemed probable of vesting. The expense is expected to be recognized over a weighted average period of 1.2 years.
Restricted Stock Units
RSU’s issued under the plans vest on a pro-rata basis on each anniversary of the issuance date over three or four years or vest in accordance with performance-based criteria. The RSU’s with performance-based vesting criteria vest in tranches contingent upon the achievement of pre-determined corporate milestones related primarily to the development of our products and the achievement of certain prescribed clinical and regulatory objectives. RSU’s with performance-based vesting criteria not vested after five years from the date of grant automatically expire. There is no consideration payable on the vesting or exercise of RSU’s issued under the plans. Upon vesting, the RSU’s are exercised automatically and settled in shares of our common stock.
Information related to RSU’s at June 30, 2011 and activity in the six months then ended is as follows:
                         
            Weighted        
            Average        
            Remaining        
            Contractual        
    Number of     Life     Aggregate  
    Units     (Years)     Intrinsic Value  
Outstanding at December 31, 2010
    544,865                  
Granted
    65,450                  
Vested/Exercised
    (29,692 )                
Forfeited
    (18,905 )                
Expired
                     
 
                     
Outstanding at June 30, 2011
    561,718       1.42     $ 41,612,069  
 
                     
Exercisable at June 30, 2011
              $  
 
                     
The aggregate intrinsic value at June 30, 2011 noted in the table above represents the closing price of our common stock traded on NASDAQ, multiplied by the number of RSU’s outstanding.
At June 30, 2011, 56,257 of the 561,718 RSU’s outstanding that are not yet exercisable are subject to performance-based vesting criteria as described above.
The total intrinsic value of RSU’s vested in the six months ended June 30, 2011 and 2010 was approximately $2.5 million and $2.6 million, respectively.
The fair value of each RSU award equals the closing price of our common stock on the date of grant. The weighted average grant date fair value per share of RSU’s granted in the six months ended June 30, 2011 and 2010 was $78.77 and $55.33, respectively.
At June 30, 2011, we had approximately $16.6 million of unrecognized compensation cost related to non-vested RSU awards, including awards not yet deemed probable of vesting. The expense is expected to be recognized over a weighted average period of 1.3 years.
XML 39 R2.htm IDEA: XBRL DOCUMENT  v2.3.0.11
Condensed Consolidated Balance Sheets (Unaudited) (USD $)
Jun. 30, 2011
Dec. 31, 2010
Current assets:    
Cash and cash equivalents $ 118,843,674 $ 192,148,312
Short-term investments, net 79,998,132 21,330,110
Accounts receivable, net 15,248,062 19,052,672
Inventories, net 22,522,356 15,076,590
Prepaid expenses and other current assets 4,659,251 2,406,505
Total current assets 241,271,475 250,014,189
Property, plant and equipment, net 11,130,352 7,484,022
Long-term investments, net 0 4,005,659
Other intangible assets, net 1,785,509 1,595,456
Deferred financing costs, net 2,800,497 2,939,149
Restricted cash 1,538,429 1,538,429
Total assets 258,526,262 267,576,904
Current liabilities:    
Accounts payable 3,336,590 3,889,643
Accrued expenses and other current liabilities 8,331,089 7,001,350
Total current liabilities 11,667,679 10,890,993
Convertible senior notes, net 91,518,710 88,921,557
Commitments and contingencies - See Note 16    
Stockholders' equity:    
Preferred stock - $.001 par value; 5,000,000 shares authorized; no shares issued and outstanding at June 30, 2011 and December 31, 2010 0 0
Common stock - $.001 par value; 25,000,000 shares authorized; 13,925,984 and 13,878,686 shares issued and outstanding at June 30, 2011 and December 31, 2010, respectively 13,926 13,879
Additional paid-in capital 309,569,724 302,533,344
Accumulated deficit (146,795,591) (127,268,545)
Accumulated other comprehensive loss:    
Cumulative translation adjustments (7,457,261) (7,548,706)
Unrealized gain on investments 9,075 34,382
Total accumulated other comprehensive loss (7,448,186) (7,514,324)
Total stockholders' equity 155,339,873 167,764,354
Total liabilities and stockholders' equity $ 258,526,262 $ 267,576,904
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