510(k) K173189 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Lumfuse TP
| Applicant | Precifit Medical, Ltd., St Paul MN, US |
| Decision | Substantially Equivalent, Jun 8, 2018 |
| Received | Oct 2, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173189
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.