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 |