G7® Vivacit-E® Freedom® Constrained Liner

G7® Vivacit-E® Freedom® Constrained Liner is an FDA 510(k)-cleared medical device (K212512) manufactured by Zimmer, 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 April 27, 2022. Regulation: 8.