Anteralign(TM) Spinal System with Titan NanoLOCK Surface Technology Navigated Instruments

Anteralign(TM) Spinal System with Titan NanoLOCK Surface Technology Navigated Instruments is an FDA 510(k)-cleared medical device (K221180) 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 May 24, 2022. Regulation: 8.