VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System

VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System is an FDA 510(k)-cleared medical device (K180822) manufactured by Wenzel Spine, 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 January 27, 2019. Regulation: 8.