510(k) K254061 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Curiteva Porous PEEK Cervical Interbody Fusion System
| Applicant | Curiteva, Inc., Tanner AL, US |
| Decision | Substantially Equivalent, Jan 15, 2026 |
| Received | Dec 17, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K254061
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.