ANATOMICAL SHOULDER INVERSE/REVERSE

ANATOMICAL SHOULDER INVERSE/REVERSE is an FDA 510(k)-cleared medical device (K053274) manufactured by Zimmer GmbH. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 24, 2006. Regulation: 8.