510(k) K192248 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Cortina [MAX] Lumbar Cage System
| Applicant | Neurostructures, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Nov 25, 2019 |
| Received | Aug 19, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192248
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.