510(k) K252737 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
DeGen Medical Latitude-C AM Cervical Interbody Fusion System
| Applicant | Degen Medical, Florence SC, US |
| Decision | Substantially Equivalent, Oct 10, 2025 |
| Received | Aug 28, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252737
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.