Trident II Acetabular System

Trident II Acetabular System is an FDA 510(k)-cleared medical device (K191358) manufactured by Howmedica Osteonics Corp. A.K.A. 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 October 23, 2019. Regulation: 8.