510(k) K052181 ยท KWP Appliance, Fixation, Spinal Interlaminal
MODIFICATION TO XIA SPINAL SYSTEM
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Sep 8, 2005 |
| Received | Aug 10, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052181
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.