510(k) K230851 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Kodiak Lumbar Spacer System
| Applicant | Met One Technologies, LLC, El Paso TX, US |
| Decision | Substantially Equivalent, May 26, 2023 |
| Received | Mar 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230851
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.