510(k) K191516 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Ali Interbody Fusion System
| Applicant | Raed M. Ali, M.D., Inc., Newport Coast CA, US |
| Decision | Substantially Equivalent, Sep 12, 2019 |
| Received | Jun 7, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191516
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.