Artisan Bone Plug, Universal Cement Restrictor

Artisan Bone Plug, Universal Cement Restrictor is an FDA 510(k)-cleared medical device (K220838) manufactured by Howmedica Osteonics, Dba Stryker Orthopaedics. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 19, 2022. Regulation: 8.