510(k) K213030 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, Feb 13, 2023 |
| Received | Sep 21, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213030
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.