510(k) K010181 ยท KWP Appliance, Fixation, Spinal Interlaminal
CD HORIZON SPINAL SYSTEM, 4.5 ROD FOR POSTERIOR APPLICATION
| Applicant | Medtronic Sofamor Danek, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Jun 12, 2001 |
| Received | Jan 19, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010181
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.