This page includes the latest FDA filings for Atricure Minneapolis. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3011788769 |
| FEI Number | 3011788769 |
| Name | AtriCure - Minneapolis |
| Owner & Operator | ATRICURE, INC. |
| Contact Address | 7555 Innovation Way -- Mason OH 45040 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 130 Cheshire Ln Ste 250 Minnetonka, MN 55305 US |
| Establishment Type | Develop Specifications But Do Not Manufacture At This Facility |
Device Company | Device | Date |
|---|---|---|
AtriCure - Minneapolis [ATRICURE, INC.] | AtriCure cryoICE cryoFORM cryoablation probe (CRYOF) | 2016-03-25 |
AtriCure - Minneapolis [ATRICURE, INC.] | CRYO3 - AtriCure cryoICE cryo-ablation probe | 2015-04-03 |