510(k) K930009 ยท KWP Appliance, Fixation, Spinal Interlaminal
STRYKER 2S SPINAL SYSTEM
| Applicant | Stryker Corp., 59 Route 17 NJ, US |
| Decision | Substantially Equivalent, Sep 1, 1994 |
| Received | Jan 4, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930009
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.