Renovis S141 Lumbar Interbody Fusion System

Renovis S141 Lumbar Interbody Fusion System is an FDA 510(k)-cleared medical device (K170888) 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 August 7, 2017. Regulation: 8.