510(k) K240889 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ARTFX Lumbar PEEK Cages
| Applicant | Artfx Medical, Jacksonville FL, US |
| Decision | Substantially Equivalent, Oct 2, 2024 |
| Received | Apr 1, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240889
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.