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ATS Medical Announces Fourth Quarter and Full Year 2009 Results
Date:3/1/2010

  • In December 2009, the Company received CE Mark of its ATS 3f Enable Bioprosthesis for commercialization in the European Union. The Enable valve combines the ATS 3f Aortic Bioprosthesis with over eight years of proven clinical performance and a self-expanding Nitinol™ frame to hold the valve in its optimal position eliminating the need for conventional sutures.  This design allows the Enable valve to be folded into a small diameter and placed through a minimally invasive incision.  Commercialization of the first generation Enable valve will be limited to a controlled market release at select surgical centers in Europe.
  • The Company expects to begin commercialization of its second generation Enable valve in the second half of 2010.  The second generation Enable will provide the basis for expansion of the Enable platform into a full market release.
  • The Company is continuing to develop its sutureless tissue valve technology for use in beating heart procedures based in part on the characteristics of the next generation Enable valves.  First-in-human clinical studies of this novel technology is targeted to occur during 2010. European commercialization of a beating heart solution could occur within one to two years thereafter.

Heart Valve Repair


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SOURCE ATS Medical, Inc.
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