510(k) K162999 ยท HCG Device, Neurovascular Embolization
V-Grip Detachment Controller for use with Hydrocoil Embolic System and MicroPlex Coil System, AZUR Detachment Controller for use with AZUR Peripheral Coil System
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Mar 29, 2017 |
| Received | Oct 28, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162999
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.