510(k) K090048 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ASFORA BULLET CAGE SYSTEM
| Applicant | Medical Designs, LLC, Sioux Falls SD, US |
| Decision | Substantially Equivalent, Aug 14, 2009 |
| Received | Jan 7, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090048
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.