Comprehensive® Convertible Glenoid - Vivacit-E Liner

Comprehensive® Convertible Glenoid - Vivacit-E Liner is an FDA 510(k)-cleared medical device (K211729) manufactured by Biomet Manufacturing Corp. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 3, 2021. Regulation: 8.