510(k) K190092 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
UNiD Patient specific 3D printed TLIF cage
| Applicant | Medicrea International SA, Rillieux-La-Pape, FR |
| Decision | Substantially Equivalent, May 8, 2019 |
| Received | Jan 18, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190092
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.