510(k) K091122 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DIANA FUSION CAGE
| Applicant | Signus Medical, Washington DC, US |
| Decision | Substantially Equivalent, Sep 18, 2009 |
| Received | Apr 17, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091122
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.