510(k) K251444 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Endoskeleton Interbody Systems
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Sep 4, 2025 |
| Received | May 9, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251444
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.