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FDA clears GORE PROPATEN Vascular Graft

The U.S. Food & Drug Administration (FDA) has given W. L. Gore & Associates, Inc. (GORE) clearance to market its GORE PROPATEN Vascular Graft for peripheral use, including lower-limb bypass and dialysis access surgery.

The GORE PROPATEN Vascular Graft is coated with the Carmeda® bioactive surface (CBAS®) and is the first ePTFE vascular graft that reduces thrombosis or clotting. It is designed to address the clinical problem of thrombotic vascular graft failure.

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