The following data is part of a premarket notification filed by Penumbra, Inc. with the FDA for Penumbra Smart Coil.
| Device ID | K143218 |
| 510k Number | K143218 |
| Device Name: | Penumbra Smart Coil |
| Classification | Device, Neurovascular Embolization |
| Applicant | Penumbra, Inc. 1351 Harbor Bay Parkway Alameda, CA 94502 |
| Contact | Charles Denault |
| Correspondent | Charles Denault Penumbra, Inc. 1351 Harbor Bay Parkway Alameda, CA 94502 |
| Product Code | HCG |
| CFR Regulation Number | 882.5950 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-11-10 |
| Decision Date | 2015-03-18 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PENUMBRA SMART COIL 86325514 4847087 Live/Registered |
Penumbra, Inc. 2014-07-01 |