Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee

Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee is an FDA 510(k)-cleared medical device (K222056) manufactured by Howmedica Osteonics Corp., Dba Stryker Orthopaedics. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 25, 2023. Regulation: 8.