510(k) K242589 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Scarlet® AL-T
| Applicant | Spineart SA, Plan-Les-Ouates, CH |
| Decision | Substantially Equivalent, Oct 23, 2024 |
| Received | Aug 30, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242589
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.