510(k) K200048 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MectaLIF Anterior Simple
| Applicant | Medacta International S.A., Castel San Pietro (Ch), CH |
| Decision | Substantially Equivalent, Mar 9, 2020 |
| Received | Jan 9, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200048
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.