510(k) K102886 ยท KWP Appliance, Fixation, Spinal Interlaminal
CD HORIZON SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Jan 26, 2011 |
| Received | Sep 30, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102886
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.