510(k) K180431 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Cortina [MAX] Lumbar Cage System
| Applicant | Neurostructures, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Mar 22, 2018 |
| Received | Feb 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180431
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.