MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK™

MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK™ is an FDA 510(k)-cleared medical device (K172212) manufactured by Ctl Medical Corporation. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 8, 2018. Regulation: 8.