Renovis Anterior Cervical Plate System

Renovis Anterior Cervical Plate System is an FDA 510(k)-cleared medical device (K152193) manufactured by Renovis Surgical Technologies, 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 September 24, 2015. Regulation: 8.