510(k) K120816 ยท KRD Device, Vascular, For Promoting Embolization
INZONE DETACHMENT SYSTEM
| Applicant | Stryker, Fremont CA, US |
| Decision | Substantially Equivalent, Apr 17, 2012 |
| Received | Mar 19, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120816
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.