Klassic Knee System Tibial Inserts, PS-Max

Klassic Knee System Tibial Inserts, PS-Max is an FDA 510(k)-cleared medical device (K202740) manufactured by Total Joint Orthopedics, 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 October 8, 2020. Regulation: 8.