Triathlon® Hinge Knee System

Triathlon® Hinge Knee System is an FDA 510(k)-cleared medical device (K251665) 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 July 24, 2025. Regulation: 8.