510(k) K223731 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
NuVasive Modulus-C Interbody System
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jan 12, 2023 |
| Received | Dec 13, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K223731
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.