510(k) K181048 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Neo Cage System TM
| Applicant | Neo Medical SA, Villette (Lavaux), CH |
| Decision | Substantially Equivalent, Jan 29, 2019 |
| Received | Apr 19, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181048
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.