FLIXENE IFG VASCULAR GRAFT

FLIXENE IFG VASCULAR GRAFT is an FDA 510(k)-cleared medical device (K130142) manufactured by Atrium Medical Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 14, 2013. Regulation: 8.