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# Wenzel Spine VariLift-LX Gains Clearance
- URL: https://www.fdaweb.com/wenzel-spine-varilift-lx-gains-clearance/
- Published: 2016-02-11T12:00:00.000Z
- Updated: 2026-09-15T02:35:10.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5134743

> FDA has cleared a Wenzel Spine 510(k) to market VariLift-LX as an interbody fusion device for stand-alone use in the lumbar spine. The device is designed to “simplify” to be implanted in a unilateral or bilateral capacity, it says. It has four large fenestrations and a bone graft chamber to promote vertebral fusion.