G7 Dual Mobility System, Active Articulation System

G7 Dual Mobility System, Active Articulation System is an FDA 510(k)-cleared medical device (K161190) manufactured by Biomet, 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 May 25, 2016. Regulation: 8.