510(k) K041217 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MODIFICATION TO BONE GRAFT WASHER
| Applicant | Medtronic Sofamor Danek, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, May 28, 2004 |
| Received | May 10, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041217
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.