POROCOAT DUAL-LOCK TOTAL HIP SYSTEM

POROCOAT DUAL-LOCK TOTAL HIP SYSTEM is an FDA 510(k)-cleared medical device (K830004) 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 April 18, 1983. Regulation: 8.