510(k) K100037 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ADVANCED VERTEBRAL SOLUTIONS EXPRESS BFD
| Applicant | Advanced Vertebral Solutions, LLC, Ambler PA, US |
| Decision | Substantially Equivalent, Sep 23, 2010 |
| Received | Jan 6, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100037
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.