REPICCI II UNICONDYLAR KNEE ALL POLY TIBIAL COMPONENTS

REPICCI II UNICONDYLAR KNEE ALL POLY TIBIAL COMPONENTS is an FDA 510(k)-cleared medical device (K980665) 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 May 19, 1998. Regulation: 8.