510(k) K122637 ยท FST Light, Surgical, Fiberoptic
LITE DECOMPRESSION SYSTEM- LIGHT CABLE MODEL 48089999
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Nov 1, 2012 |
| Received | Aug 29, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122637
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.