510(k) K151374 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
NuVasive MLX-Medial Lateral Expandable Lumbar Interbody System, NuVasive AP Expandable XLIF System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Aug 6, 2015 |
| Received | May 22, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151374
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.