510(k) K140564 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
BN LUMBAR CAGE SYSTEM
| Applicant | Medyssey USA, Inc., Fr. Myers FL, US |
| Decision | Substantially Equivalent, Jun 5, 2014 |
| Received | Mar 5, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140564
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.