510(k) K232530 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Stable-L Standalone Lumbar Interbody System, Stable-C Interbody System
| Applicant | Nexus Spine, LLC, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Sep 18, 2023 |
| Received | Aug 21, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232530
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.