510(k) K112696 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TWIN PEAKS LUMBAR CAGE
| Applicant | Qualgenix, LLC, Oxford CT, US |
| Decision | Substantially Equivalent, Apr 18, 2012 |
| Received | Sep 15, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112696
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.