FortiBridge Anterior Cervical Plate System

FortiBridge Anterior Cervical Plate System is an FDA 510(k)-cleared medical device (K162250) manufactured by Nanovis Spine, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 25, 2016. Regulation: 8.