510(k) K162431 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Luna 3D Interbody Fusion System
| Applicant | Benvenue Medical, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Nov 17, 2016 |
| Received | Aug 31, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162431
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.