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InspireMD Receives CE Mark Approval for Carotid Embolic Protection Stent
Date:3/15/2013

cations challenges, burdens and costs of compliance with foreign laws and political and economic instability in each jurisdiction. More detailed information about the Company and the risk factors that may affect the realization of forward-looking statements is set forth in the Company's filings with the Securities and Exchange Commission (SEC), including the Company's Transition Report on From 10-K/T and its Quarterly Reports on Form 10-Q.  Investors and security holders are urged to read these documents free of charge on the SEC's web site at http://www.sec.gov. The Company assumes no obligation to publicly update or revise its forward-looking statements as a result of new information, future events or otherwise.

For additional information:
InspireMD Desk
Redington Inc.,
+1-212-926-1733
+1-203-222-7399
inspiremd@redingtoninc.com
 
Company Contact:
Jonina Ohayon
Marketing Director
jonina@inspiremd.com
OTC BB: NSPR



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SOURCE InspireMD, Inc.
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Related medicine technology :

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2. InspireMD Reports Results for Period Ended Dec. 31, 2012
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4. Positive Results of InspireMDs MASTER Trial to be Published on November 6 in Journal of American College of Cardiology
5. InspireMD Reports Results For Period Ending Sept. 30, 2012
6. InspireMD Announces Positive Results From MGuard(TM) Stent MASTER Trial for Emergency Treatment of Heart Attack Patients
7. InspireMD to Present at Harvard Investors Group on June 27 in New York
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9. InspireMD Announces Positive 3-Year Results from Extended MAGICAL trial
10. InspireMD Announces First Quarter 2012 Financial Results
11. Cardium Receives ISO Certification for Excellagen
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