Navigated Disc Prep Instruments and CAPSTONE Trials

Navigated Disc Prep Instruments and CAPSTONE Trials is an FDA 510(k)-cleared medical device (K150231) manufactured by Medtronic Sofamor Danek USA, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 15, 2015. Regulation: 8.