POWEReam 1/4 Drive

POWEReam 1/4 Drive is an FDA 510(k)-cleared medical device (K233300) manufactured by Stryker Instruments. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 25, 2023. Regulation: 8.