510(k) K111719 ยท KWP Appliance, Fixation, Spinal Interlaminal
OASYS SPINAL SYSTEM
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Jan 19, 2012 |
| Received | Jun 20, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K111719
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.