DeGen Medical Latitude-C AM Cervical Interbody Fusion System

DeGen Medical Latitude-C AM Cervical Interbody Fusion System is an FDA 510(k)-cleared medical device (K252737) manufactured by Degen Medical. 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 9, 2025. Regulation: 8.