Univers Revers CA Head and Adapter

Univers Revers CA Head and Adapter is an FDA 510(k)-cleared medical device (K233260) 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 February 11, 2024. Regulation: 8.