REPICCI II UNICONDYLAR KNEE

REPICCI II UNICONDYLAR KNEE is an FDA 510(k)-cleared medical device (K971938) 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 August 24, 1997. Regulation: 8.