510(k) K172341 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
NuVasive® Modulus TLIF Interbody System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Oct 26, 2017 |
| Received | Aug 2, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172341
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.