510(k) K153105 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MLX - Medial Lateral Expandable Lumbar Interbody System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Jul 11, 2016 |
| Received | Oct 27, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153105
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.