MLX - MEDIAL LATERAL EXPANDABLE LUMBAR INTERBODY SYSTEM

MLX - MEDIAL LATERAL EXPANDABLE LUMBAR INTERBODY SYSTEM is an FDA 510(k)-cleared medical device (K140770) 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 24, 2014. Regulation: 8.