Arthrex VaultLock Glenoid

Arthrex VaultLock Glenoid is an FDA 510(k)-cleared medical device (K161108) 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 28, 2016. Regulation: 8.