INTESS CERVICAL CAGE SYSTEM

INTESS CERVICAL CAGE SYSTEM is an FDA 510(k)-cleared medical device (K133815) manufactured by Kalitec Direct, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 15, 2014. Regulation: 8.