510(k) K961633 ยท KWP Appliance, Fixation, Spinal Interlaminal
CD HORIZON SPINAL SYSTEM
| Applicant | Sofamor Danek USA,Inc., Memphis TN, US |
| Decision | Substantially Equivalent for Some Indications, Dec 5, 1996 |
| Received | Apr 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961633
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.