510(k) K251016 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MectaLIF 3D Metal
| Applicant | Medacta International S.A., Castel San Pietro, CH |
| Decision | Substantially Equivalent, Jul 17, 2025 |
| Received | Apr 2, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251016
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.