Adaptix™ Interbody System with Titan nanoLOCK™ Surface Technology

Adaptix™ Interbody System with Titan nanoLOCK™ Surface Technology is an FDA 510(k)-cleared medical device (K250669) 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 April 21, 2025. Regulation: 8.