510(k) K231735 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
NuVasive CoRoent Small Interbody System; NuVasive CoRoent Small Contoured Interbody System; NuVasive CoRoent Small Interlock System; NuVasive CoRoent Small Interlock II System; NuVasive CoRoent Small Ti-C System; NuVasive Cohere Cervical Interbody System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Jul 11, 2023 |
| Received | Jun 14, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231735
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.