Catalyft LS Expandable Interbody System with Titan nanoLOCK Surface Technology

Catalyft LS Expandable Interbody System with Titan nanoLOCK Surface Technology is an FDA 510(k)-cleared medical device (K223153) 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 December 15, 2022. Regulation: 8.