510(k) K193172 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Luna XD Ti Interbody Fusion System
| Applicant | Benvenue Medical, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Jul 2, 2020 |
| Received | Nov 15, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193172
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.