510(k) K212831 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MectaLIF Extension
| Applicant | Medacta International S.A., Castel San Pietro, CH |
| Decision | Substantially Equivalent, Oct 29, 2021 |
| Received | Sep 7, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212831
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.