Stryker Orthopaedics Hip Devices Labeling Update

Stryker Orthopaedics Hip Devices Labeling Update is an FDA 510(k)-cleared medical device (K243784) 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 February 5, 2025. Regulation: 8.