510(k) K141135 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
JULIET LL
| Applicant | Spineart, Geneva, CH |
| Decision | Substantially Equivalent, Dec 1, 2014 |
| Received | May 1, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141135
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.