510(k) K082342 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MODIFICATION TO CAPSTONE SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Sep 12, 2008 |
| Received | Aug 15, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082342
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.