510(k) K173782 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
UNiD Patient Specific 3D printed cage
| Applicant | Medicrea International SA, Rillieux-La-Pape, FR |
| Decision | Substantially Equivalent, Apr 25, 2018 |
| Received | Dec 13, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173782
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.