Stryker and Serf hip devices

Stryker and Serf hip devices is an FDA 510(k)-cleared medical device (K250989) 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.