510(k) K250667 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DeGen Medical Patient Specific Implant (PSI) System
| Applicant | Degen Medical, Florence SC, US |
| Decision | Substantially Equivalent, Apr 4, 2025 |
| Received | Mar 5, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K250667
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.