CONSENSUS FEMORAL COMPONENT, POROUS, COCR/TI

CONSENSUS FEMORAL COMPONENT, POROUS, COCR/TI is an FDA 510(k)-cleared medical device (K983004) manufactured by Hayes Medical, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 24, 1998. Regulation: 8.