NuVasive(R) CCX-L Interbody System

NuVasive(R) CCX-L Interbody System is an FDA 510(k)-cleared medical device (K143595) manufactured by Nu Vasive, Incorporated. 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 28, 2015. Regulation: 8.