510(k) K201692 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
NuVasive Modulus XLIF Interbody System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Oct 29, 2020 |
| Received | Jun 22, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201692
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.