510(k) K142023 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LUNA INTERBODY SYSTEM
| Applicant | Benvenue Medical, Inc., Hillsborough CA, US |
| Decision | Substantially Equivalent, Nov 20, 2014 |
| Received | Jul 25, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142023
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.