Arthrex Univers Revers Porous Coated Baseplate and Universal Glenoid Inlay

Arthrex Univers Revers Porous Coated Baseplate and Universal Glenoid Inlay is an FDA 510(k)-cleared medical device (K182039) 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 September 27, 2018. Regulation: 8.