510(k) K091638 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DORADO WIDE INTERVERTEBRAL BODY CAGE, MODELS: IM2010-IM2031
| Applicant | Spinefrontier, Inc., Beverly MA, US |
| Decision | Substantially Equivalent, Sep 14, 2009 |
| Received | Jun 4, 2009 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K091638
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.