The following data is part of a premarket notification filed by Wallaby Medical, Inc. with the FDA for Wallaby Avenir Coil System.
Device ID | K173711 |
510k Number | K173711 |
Device Name: | Wallaby Avenir Coil System |
Classification | Device, Neurovascular Embolization |
Applicant | Wallaby Medical, Inc. 23181 Verdugo Dr. Laguna Hills, CA 92653 |
Contact | Rebecca K. Pine |
Correspondent | Rebecca K. Pine Wallaby Medical, Inc. 23181 Verdugo Dr. Laguna Hills, CA 92653 |
Product Code | HCG |
CFR Regulation Number | 882.5950 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-12-04 |
Decision Date | 2018-05-04 |
Summary: | summary |