510(k) K181970 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MectaLIF Posterior Extension
| Applicant | Medacta International S.A., Castel San Pietro (Ch), CH |
| Decision | Substantially Equivalent, Dec 4, 2018 |
| Received | Jul 24, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181970
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.