POROCOAT MARK II TOTAL ELBOW

POROCOAT MARK II TOTAL ELBOW is an FDA 510(k)-cleared medical device (K872084) manufactured by Depuy, 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 June 24, 1987. Regulation: 8.