510(k) K182158 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
UNiD Patient-matched PLIF cage
| Applicant | Medicrea International SA, Rillieux-La-Pape, FR |
| Decision | Substantially Equivalent, Jul 15, 2019 |
| Received | Aug 9, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182158
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.