Current Report Filing (8-k)
June 29 2015 - 3:44PM
Edgar (US Regulatory)
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant
to Section 13 or 15(d)
of The Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): June 29, 2015
(Date of earliest event reported)
ABIOMED, Inc.
(Exact name of registrant as specified in its charter)
|
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| Delaware |
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04-2743260 |
| (State or other Jurisdiction
of Incorporation) |
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(IRS Employer
Identification Number) |
001-09585
(Commission File Number)
22 Cherry Hill Drive
Danvers, MA 01923
(Address of Principal Executive Offices, including Zip Code)
(978) 646-1400
(Registrant’s Telephone Number, including Area Code)
Not Applicable
(Former
Name or Former Address, if Changed Since Last Report)
Check the appropriate box below
if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
| ¨ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
| ¨ |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
| ¨ |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| ¨ |
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c) |
On June 29, 2015, ABIOMED, Inc. issued a press release reporting
that it has received confirmation from the United States Department of Justice that it has closed its investigation into the Company’s marketing of the Impella® 2.5 device without taking enforcement action. The United States Department of
Justice initiated an investigation on October 26, 2012 and was seeking documents from the Company related to its marketing and labeling of the Impella® 2.5 device. A copy of the press release
is set forth as Exhibit 99.1 and is incorporated herein by reference.
| Item 9.01 |
Financial Statements and Exhibits. |
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| Number |
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Description |
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| 99.1 |
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Press release dated June 29, 2015 |
SIGNATURES
Pursuant to 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.
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| Abiomed, Inc. |
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| By: |
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/s/ Robert L. Bowen |
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Robert L. Bowen |
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Vice President and Chief Financial Officer |
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(Principal Accounting and Financial Officer) |
Date: June 29, 2015
Exhibit 99.1
UNITED STATES DEPARTMENT OF JUSTICE CLOSES INVESTIGATION INTO ABIOMED’S IMPELLA 2.5
DANVERS, MA – June 29, 2015 – Abiomed, Inc. (NASDAQ: ABMD), a leading provider of breakthrough heart support technologies, today
announced that it has received confirmation from the United States Department of Justice that it has closed its investigation into the company’s marketing of the Impella® 2.5 device
without taking enforcement action.
“We are pleased that the Department of Justice has chosen to close its investigation without pursuing any further
action and that this matter is now behind us. We have always remained steadfast in our integrity and our commitment to putting our patients first,” said Michael R. Minogue, Chairman, President, Chief Executive Officer, Abiomed.
On October 26, 2012, Abiomed was informed that the United States Attorney’s Office for the District of Columbia had initiated an investigation and
was seeking documents from the company related to its marketing and labeling of the Impella 2.5. Abiomed has cooperated fully with the government inquiry since its inception.
ABOUT ABIOMED
Based in Danvers, Massachusetts, Abiomed,
Inc., is a leading provider of medical devices that provide circulatory support. Our products are designed to enable the heart to rest by improving blood flow and/or performing the pumping of the heart. For additional information please visit:
www.abiomed.com.
FORWARD-LOOKING STATEMENTS
This release contains forward-looking statements, including statements regarding development of Abiomed’s existing and new products, the Company’s
progress toward commercial growth, and future opportunities and expected regulatory approvals. The Company’s actual results may differ materially from those anticipated in these forward-looking statements based upon a number of factors,
including uncertainties associated with development, testing and related regulatory approvals, including the potential for future losses, complex manufacturing, high quality requirements, dependence on limited sources of supply, competition,
technological change, government regulation, litigation matters, future capital needs and uncertainty of additional financing, and other risks and challenges detailed in the Company’s filings with the Securities and Exchange Commission,
including the most recently filed Annual Report on Form 10-K. Readers are cautioned not to place undue reliance on any forward-looking statements, which speak only as of the date of this release. The Company undertakes no obligation to publicly
release the results of any revisions to these forward-looking statements that may be made to reflect events or circumstances that occur after the date of this release or to reflect the occurrence of unanticipated events.
For more information, please contact:
Aimee Genzler
Director, Corporate Communications
978-646-1553
agenzler@abiomed.com
Ingrid Goldberg
Director, Investor Relations
igoldberg@abiomed.com
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