510(k) K122591 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CLYDESDALE SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Sep 18, 2012 |
| Received | Aug 24, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122591
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.