510(k) K221751 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
NuVasive Cohere ALIF System Intervertebral Body Fusion Device
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Oct 21, 2022 |
| Received | Jun 16, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221751
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.