510(k) K090353 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PERIMETER INTERBODY FUSION DEVICE
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Sep 29, 2009 |
| Received | Feb 11, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090353
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.