Wenzel Spine Lands FDA Clearance

The FDA has greenlighted Wenzel Spine’s VariLift-LX as an interbody fusion device for stand-alone use in the lumbar spine, the company announced.

The product is Wenzel’s next generation, zero-profile, stand-alone, expandable interbody fusion device.

VariLift-LX will be available in the U.S. through a limited release in the coming weeks. A full launch is planned in early spring. — Jonathon Shacat