510(k) K993067 ยท KWP Appliance, Fixation, Spinal Interlaminal
SILHOUETTE SPINAL FIXATION SYSTEM
| Applicant | Sulzer Spine-Tech, Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 16, 1999 |
| Received | Sep 13, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K993067
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.