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Home » Wenzel Spine Lands FDA Clearance
Wenzel Spine Lands FDA Clearance
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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
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