510(k) K093015 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
BINDER INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Binder Biomedical, Inc., Boca Raton FL, US |
| Decision | Substantially Equivalent, Feb 25, 2010 |
| Received | Sep 29, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093015
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.