510(k) K183092 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Kuros TLIF Cage
| Applicant | Kuros Biosciences B.V, Bilthoven, NL |
| Decision | Substantially Equivalent, Mar 8, 2019 |
| Received | Nov 7, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183092
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.