Edwards Lifesciences wins FDA approval for new heart valve

Mon. May 11, 2009; Posted: 01:24 PM

May 11, 2009 (Datamonitor via COMTEX) -- EW | Quote | Chart | News | PowerRating -- Edwards Lifesciences, a developer of heart valves, has received approval from the FDA for the Carpentier-Edwards Perimount Magna Ease aortic valve. The company plans to introduce this valve, as well as the Port Access EndoDirect minimally invasive surgery system by May 15, 2009.

The new valve includes a low profile and smooth commissure posts to ease insertion through small incisions or small aortic roots, the company said.

According to Edwards Lifesciences, Port Access EndoDirect system allows cardiac surgeons to stop a patient's heart and keep it at rest for the duration of the heart valve procedure without an incision down the middle of the chest. In procedures such as mitral valve repair and replacement, the EndoDirect system provides a minimally invasive alternative for direct aortic cannulation when femoral access is not an option.

Donald Bobo, Jr, corporate vice president of heart valve therapy at Edwards Lifesciences, said: "Edwards's new offerings are designed to give cardiac surgeons additional choices in tailoring procedures based on their preferred surgical approach and the needs of their patients."

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For full details on Edwards Life Sciences (EW) click here. Edwards Life Sciences (EW) has Short Term PowerRatings of 4. Details on Edwards Life Sciences (EW) Short Term PowerRatings is available at This Link.

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