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: LIVEWIRE(R) CARDIAC ABLATION SYSTEM
• Generic Name: Cardiac ablation percutaneous catheter
• Applicant: St Jude Medical; 14900 Minnetonka Ind Rd.; Minnetonka, MN 55345
• PMA Number: P960016
• Supplement Number: S061
• Date Received: 02/19/2016
• Decision Date: 02/29/2016
• Product Code: LPB
• Advisory Committee: Cardiovascular
• Supplement Type: 30-Day Notice
• Supplement Reason: Process Change - Manufacturer/Sterilizer/Packager/Supplier
• Expedited Review Granted?: No
• Combination Product: No
• Predetermined Change Control Plan Authorized: No

Approval Order Statement  
Acceptance of an automated process for Ampere Generator region configuration.