SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE

SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K083118) manufactured by Spinal USA. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 26, 2009. Regulation: 8.