VySpine lumbar fusion device gets FDA clearance

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

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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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