510(k) K050189 ยท KWP Appliance, Fixation, Spinal Interlaminal
TECHTONIX SYSTEM
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Feb 16, 2005 |
| Received | Jan 27, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050189
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.