510(k) K230894 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
NuVasive Modulus ALIF System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Jun 16, 2023 |
| Received | Mar 31, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230894
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.