NuVasive PEEK Corpectomy System

NuVasive PEEK Corpectomy System is an FDA 510(k)-cleared medical device (K151167) 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 September 2, 2015. Regulation: 8.