Univers Revers Modular Glenoid System, Half Augment Baseplate

Univers Revers Modular Glenoid System, Half Augment Baseplate is an FDA 510(k)-cleared medical device (K200895) manufactured by Arthrex, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 12, 2020. Regulation: 8.