Renovis A200 PS Knee System as part of the Renovis A200 Knee System

Renovis A200 PS Knee System as part of the Renovis A200 Knee System is an FDA 510(k)-cleared medical device (K190122) manufactured by Renovis Surgical Technologies. 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, 2019. Regulation: 8.