MLX™ - Medial Lateral Expandable Lumbar Interbody System

MLX™ - Medial Lateral Expandable Lumbar Interbody System is an FDA 510(k)-cleared medical device (K153105) manufactured by Nu Vasive, Incorporated. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 10, 2016. Regulation: 8.