510(k) K250845 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Curiteva Porous PEEK Standalone ALIF System
| Applicant | Curiteva, Inc., Tanner AL, US |
| Decision | Substantially Equivalent, Jun 18, 2025 |
| Received | Mar 20, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250845
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.