MODULIF-A Anterior Lumbar Interbody Fusion System

MODULIF-A Anterior Lumbar Interbody Fusion System is an FDA 510(k)-cleared medical device (K200958) manufactured by Spinal Stability, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 27, 2020. Regulation: 8.