510(k) K101183 ยท KWP Appliance, Fixation, Spinal Interlaminal
MODIFICATION TO: OASYS SYSTEM
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Nov 9, 2010 |
| Received | Apr 28, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101183
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.