510(k) K243934 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Stable-L Lumbar Interbody System
| Applicant | Nexus Spine, LLC, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Apr 30, 2025 |
| Received | Dec 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243934
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.