STRUXXURE ANTERIOR CERVICAL PLATE AND SCREWS

STRUXXURE ANTERIOR CERVICAL PLATE AND SCREWS is an FDA 510(k)-cleared medical device (K133475) manufactured by Nexxt Spine, 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 December 18, 2013. Regulation: 8.