VySpine has announced FDA 510(k) clearance of its UniVy OsteoVy-Ti NanoVy-HA cervical intervertebral body fusion system, according to a press release.
The UniVy OsteoVy-Ti NanoVy-HA cervical intervertebral body fusion (IBF) system is indicated for patients with degenerative disc disease who undergo IBF at one level in the cervical spine. According to the release, the system is designed with a range of sizes, heights and lordotic angles to promote bone integration and tissue regeneration.
VySpine has announced FDA 510(k) clearance of its UniVy OsteoVy-Ti NanoVy-HA cervical intervertebral body fusion system, according to a press release.
The UniVy OsteoVy-Ti NanoVy-HA cervical intervertebral body fusion (IBF) system is indicated for patients with degenerative disc disease who undergo IBF at one level in the cervical spine. According to the release, the system is designed with a range of sizes, heights and lordotic angles to promote bone integration and tissue regeneration.
