510(k) K983706 ยท KWP Appliance, Fixation, Spinal Interlaminal
MODIFICATION OF TOWNLEY PEDICLE SCREW PLATING SYSTEM
| Applicant | Sofamor Danek USA,Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Nov 12, 1998 |
| Received | Oct 21, 1998 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K983706
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.