The following data is part of a premarket notification filed by Atricure, Inc. with the FDA for Atricure Bipolar System.
| Device ID | K110117 |
| 510k Number | K110117 |
| Device Name: | ATRICURE BIPOLAR SYSTEM |
| Classification | Surgical Device, For Cutting, Coagulation, And/or Ablation Of Tissue, Including Cardiac Tissue |
| Applicant | ATRICURE, INC. 6217 CENTER PARK DRIVE West Chester, OH 45069 |
| Contact | James Lucky, Rac |
| Correspondent | James Lucky, Rac ATRICURE, INC. 6217 CENTER PARK DRIVE West Chester, OH 45069 |
| Product Code | OCL |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-01-18 |
| Decision Date | 2011-04-08 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00818354011043 | K110117 | 000 |
| 30840143900000 | K110117 | 000 |