KINEMATIC II REPLACEMENT TIBIAL INSERTS

KINEMATIC II REPLACEMENT TIBIAL INSERTS is an FDA 510(k)-cleared medical device (K960976) manufactured by Howmedica Corp.. 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 6, 1996. Regulation: 8.