510(k) K073440 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FOUNDATION CAGE
| Applicant | Corelink, LLC, Round Rock TX, US |
| Decision | Substantially Equivalent, Apr 24, 2008 |
| Received | Dec 7, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073440
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.