VySpine, in a press statement, announced that the FDA has cleared its UniVy OsteoVy Ti NanoVy Ha cervical intervertebral bodies fusion system.
The UniVy OsteoVy Ti NanoVy Ha cervical intervertebral (IBF), system is indicated for degenerative disc disease patients who undergo IBF in one level of their cervical spine. According to a press release, this system was designed to have a range in sizes, heights and angles of lordotic to encourage bone integration and tissue repair.
