VySpine lumbar fusion device gets FDA clearance

Spinal Tech

VySpine's LumiVy NanoVy Ti lumbar interbody fusion system earned FDA clearance, the devicemaker said Jan. 17.

The device is indicated for one- and two- levels for degenerative disc disease with up to Grade 1 spondylolisthesis, according to a news release. It has a titanium coating designed to facilitate  direct osteoblast attachment to the entire surface of the implant.

The LumiVy NanoVy Ti system is available in a variety of footprints for most interbody approaches.

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