510(k) K240326 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Solar Lumbar Interbody Fusion System
| Applicant | Degen Medical, Inc., Florence SC, US |
| Decision | Substantially Equivalent, Jul 29, 2024 |
| Received | Feb 2, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240326
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.