The following data is part of a premarket notification filed by Penumbra, Inc. with the FDA for Penumbra Coil 400, Ruby Coil System, Pod System.
Device ID | K173614 |
510k Number | K173614 |
Device Name: | Penumbra Coil 400, Ruby Coil System, POD System |
Classification | Device, Neurovascular Embolization |
Applicant | Penumbra, Inc. One Penumbra Place Alameda, CA 94502 |
Contact | Aditi Kolla |
Correspondent | Aditi Kolla Penumbra, Inc. One Penumbra Place 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 | 2017-11-22 |
Decision Date | 2018-04-17 |
Summary: | summary |