510(k) K241321 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Juliet® Ti LL Lumbar Interbody Device
| Applicant | Spineart SA, Plan Les Ouates, CH |
| Decision | Substantially Equivalent, Jul 18, 2024 |
| Received | May 10, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241321
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.