510(k) K160832 ยท HCG Device, Neurovascular Embolization
Penumbra Smart Coil
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Apr 20, 2016 |
| Received | Mar 25, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K160832
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.