510(k) K200551 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MectaLIF Transforaminal TiPEEK
| Applicant | Medacta Inernational SA, Castel San Pietro (Ch), CH |
| Decision | Substantially Equivalent, Feb 12, 2021 |
| Received | Mar 3, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200551
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.