510(k) K223418 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DeGen Impulse AM System
| Applicant | Degen Medical, Florence SC, US |
| Decision | Substantially Equivalent, Mar 17, 2023 |
| Received | Nov 10, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223418
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.