510(k) K142741 ยท KWP Appliance, Fixation, Spinal Interlaminal
OASYS System
| Applicant | Stryker Corporation, Allendale NJ, US |
| Decision | Substantially Equivalent, Jan 15, 2015 |
| Received | Sep 24, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142741
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.