510(k) K261020 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Symmetrix L Spinal System
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Jul 14, 2026 |
| Received | Mar 27, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261020
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.