VySpine earned FDA clearance for its LumiVy OsteoVy PEKK lumbar interbody fusion device, according to an Oct. 9 news release.
Three notes:
1. The device was cleared for use in intervertebral body fusion at one or two contiguous levels to treat degenerative disc disease.
2. It is available in multiple footprints and heights from 6 millimeters to 21 millimeters.
3. LumiVy is made from 3D-printed OXPEKK material and has VySpine's proprietary OsteoVy lattice structure.