PMI (PATIENT MATCHED IMPLANTS) HIP FEMORAL COMP

PMI (PATIENT MATCHED IMPLANTS) HIP FEMORAL COMP is an FDA 510(k)-cleared medical device (K911802) manufactured by Biomet, 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 January 1, 1992. Regulation: 8.