510(k) K132700 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PERIMETER INTERBODY FUSION DEVICE
| Applicant | Medtronic Sofamor Danek, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Sep 26, 2013 |
| Received | Aug 29, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132700
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.