Ti-Diagon Oblique TLIF

Ti-Diagon Oblique TLIF is an FDA 510(k)-cleared medical device (K172064) manufactured by Camber Spine 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 September 14, 2017. Regulation: 8.