510(k) K201267 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Adaptix Interbody System with Titan nanoLOCK Surface Technology
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Aug 26, 2020 |
| Received | May 12, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201267
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.