CD HORIZON® Spinal System

CD HORIZON® Spinal System is an FDA 510(k)-cleared medical device (K162379) manufactured by Medtronic Sofamor Danek USA, 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 15, 2016. Regulation: 8.