Klassic Knee System - Revision Tibial Baseplate

Klassic Knee System - Revision Tibial Baseplate is an FDA 510(k)-cleared medical device (K243991) manufactured by Total Joint Othopedics, 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 March 23, 2025. Regulation: 8.