510(k) K210439 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
NuVasive MOD-EX XLIF Interbody System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, May 12, 2021 |
| Received | Feb 12, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210439
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.