510(k) K212389 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Advantage Lumbar System - ALIF, PLIF, DLIF, TLIF
| Applicant | Intelivation, LLC, Saint Simons Island GA, US |
| Decision | Substantially Equivalent, Oct 29, 2021 |
| Received | Aug 2, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212389
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.