510(k) K082732 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MODIFICATION TO: CAPSTONE SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Oct 16, 2008 |
| Received | Sep 18, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082732
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.