Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information. |
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Device | EPi-Sense® ST Guided Coagulation System |
Generic Name | Surgical cardiac ablation device, for treatment of atrial fibrillation |
Applicant | AtriCure, Inc. 7555 Innovation Way West Chester, OH 45040 |
PMA Number | P200002 |
Supplement Number | S002 |
Date Received | 02/17/2022 |
Decision Date | 08/16/2022 |
Product Code |
OCM |
Advisory Committee |
Cardiovascular |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement Approval for a modified version of the coagulation probe called EPi-Sense ST, a new radiofrequency (RF) cable for use with EPi-Sense ST, and a modified cannula for use with both EPi-Sense and EPi-Sense ST. |
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