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 |