Premarket Approval (PMA)

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.

• Device: TACTICATH QUARTZ CATHETER AND TACTISYSQUARTZ EQUIPMENT
• Generic Name: Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation
• Applicant: St. Jude Medical; One St. Jude Medical Drive; St. Paul, MN 55117
• PMA Number: P130026
• Supplement Number: S010
• Date Received: 09/23/2015
• Decision Date: 10/21/2015
• Product Code: OAE
• Advisory Committee: Cardiovascular
• Supplement Type: 30-Day Notice
• Supplement Reason: Process Change - Manufacturer/Sterilizer/Packager/Supplier
• Expedited Review Granted?: No
• Combination Product: No

Approval Order Statement  
TO REMOVE A REDUNDANT RUN-IN TEST FOR THE AMPERE SYSTEM FROM THE MANUFACTURING PROCESS.