510(k) K012173 ยท KWP Appliance, Fixation, Spinal Interlaminal
DEVICE MODIFICATION OF SILHOUETTE SPINDAL FIXATION SYSTEM
| Applicant | Sulzer Spine-Tech, Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 28, 2001 |
| Received | Jul 12, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012173
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.