VySpine receives FDA 510(k) clearance of intervertebral body fusion system

Fact checked byGina Brockenbrough, MA

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VySpine received FDA clearance of the UniVy OsteoVy-Ti NanoVy-HA cervical intervertebral body fusion system.
The system is indicated for patients undergoing fusion at one level in the cervical spine.

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.

Generic FDA News infographic — VySpine received FDA clearance of the UniVy OsteoVy-Ti NanoVy-HA cervical intervertebral body fusion system. *Image: Adobe Stock*

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VySpine receives FDA 510(k) clearance of intervertebral body fusion system

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