510(k) K050809 ยท KWP Appliance, Fixation, Spinal Interlaminal
CD HORIZON SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Jun 14, 2005 |
| Received | Mar 31, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050809
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.