510(k) K090707 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TALOS INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Meditech Advisors, LLC, Chicago IL, US |
| Decision | Substantially Equivalent, Jul 15, 2009 |
| Received | Mar 17, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090707
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.