510(k) K112648 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ASFORA BULLET CAGE
| Applicant | Medical Designs, LLC, Sioux Falls SD, US |
| Decision | Substantially Equivalent, Mar 13, 2012 |
| Received | Sep 12, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112648
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.