Renovis S180 Lateral Lumbar Interbody Fusion System

Renovis S180 Lateral Lumbar Interbody Fusion System is an FDA 510(k)-cleared medical device (K181655) 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 September 10, 2018. Regulation: 8.