510(k) K252205 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF System
| Applicant | Curiteva, Inc., Tanner AL, US |
| Decision | Substantially Equivalent, Jan 16, 2026 |
| Received | Jul 14, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252205
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.