CardioTech International

CardioTech Receives FDA Approval for Export of Second Graft Size for CardioPass Clinical Trial

Published in Medical Letter on the CDC and FDA, August 3rd, 2008

CardioTech International, Inc. (AMEX: CTE), a leading developer and manufacturer of advanced biomaterials for a broad range of medical devices, announced that it has received the necessary U.S. Food and Drug Administration ("FDA") approval to export its 4mm graft in further support of the ongoing European clinical trial of CardioPass(TM) , the Company's proprietary synthetic coronary bypass graft.

Commenting on the announcement, Michael Adams, CEO and President, said, "We are pleased with the FDA's timely review and approval of our request to export the 4mm graft for use in our CardioPass(TM) European clinical trial. This important milestone provides a second graft size...

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Source: Medical Letter on the CDC and FDA (2008-08-03)

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