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.