510(k) K123377 ยท HCG Device, Neurovascular Embolization
TARGET DETACHABLE COIL
| Applicant | Stryker Neurovascular, Fremont CA, US |
| Decision | Substantially Equivalent, Nov 30, 2012 |
| Received | Nov 1, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123377
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.