510(k) K210090 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Impulse AM Interbody Fusion System
| Applicant | Degen Medical, Florence SC, US |
| Decision | Substantially Equivalent, Aug 30, 2021 |
| Received | Jan 13, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210090
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.