510(k) K181261 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Curiteva Cervical Interbody Fusion System
| Applicant | Curiteva, LLC, Tanner AL, US |
| Decision | Substantially Equivalent, Jul 9, 2018 |
| Received | May 11, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181261
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.