VASCULAR GRAFT/BIFURCATED/FEP-RINGED

VASCULAR GRAFT/BIFURCATED/FEP-RINGED is an FDA 510(k)-cleared medical device (K830806) 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 August 12, 1983. Regulation: 8.