Tailored-C Cervical Interbody Fusion System

Tailored-C Cervical Interbody Fusion System is an FDA 510(k)-cleared medical device (K200458) manufactured by Bespoke 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 December 27, 2020. Regulation: 8.