ACTIFY™ 3D Total Knee System, ACTIFY™ Total Knee System

ACTIFY™ 3D Total Knee System, ACTIFY™ Total Knee System is an FDA 510(k)-cleared medical device (K240669) manufactured by Globus Medical, 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 June 19, 2024. Regulation: 8.