510(k) K173702 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Juliet Ti LL
| Applicant | Spineart, Plan Les Ouates, CH |
| Decision | Substantially Equivalent, Jan 3, 2018 |
| Received | Dec 4, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173702
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.