510(k) K181621 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, Oct 19, 2018 |
| Received | Jun 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181621
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.