510(k) K221172 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FOCUS Interbody System
| Applicant | Oc Medical Devices, Savannah GA, US |
| Decision | Substantially Equivalent, Oct 14, 2022 |
| Received | Apr 25, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221172
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.