510(k) K170852 ยท HCG Device, Neurovascular Embolization
POD Packing Coil
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Jul 19, 2017 |
| Received | Mar 22, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170852
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.