NEX-D2 Posterior Fixation System

NEX-D2 Posterior Fixation System is an FDA 510(k)-cleared medical device (K190981) manufactured by Next Orthosurgical. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 14, 2020. Regulation: 8.