510(k) K231763 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Stable-C Interbody System
| Applicant | Nexus Spine, LLC, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Aug 21, 2023 |
| Received | Jun 16, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231763
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.