CAMBER SPINE DIAGON OBLIQUE CAGE

CAMBER SPINE DIAGON OBLIQUE CAGE is an FDA 510(k)-cleared medical device (K134038) manufactured by Camber Spine. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 19, 2014. Regulation: 8.