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 |