ARENA-C TIFUSE CERVICAL INTERVERTEBRAL BODY FUSION DEVICE

ARENA-C TIFUSE CERVICAL INTERVERTEBRAL BODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K141333) manufactured by Spinefrontier, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 24, 2014. Regulation: 8.