GORE® PROPATEN® Vascular Graft

GORE® PROPATEN® Vascular Graft is an FDA 510(k)-cleared medical device (K232312) manufactured by W. L. Gore & Associates, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 8, 2024. Regulation: 8.