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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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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.
 
DeviceINTERSTIM LEADS
Generic NameImplanted electrical device intended for treatment of fecal incontinence
Regulation Number876.5270
ApplicantMedtronic Neuromodulation
7000 Central Ave., NE
Ms Rcw225
Minneapolis, MN 55432
PMA NumberP080025
Supplement NumberS024
Date Received12/16/2011
Decision Date01/13/2012
Product Code QON 
Advisory Committee Gastroenterology/Urology
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
ADDITION OF TWO NEW DESKTOP WELDING STATIONS WITH UPDATED POWER SUPPLIES, AND TWO PROCESS CHANGES TO INCLUDE THE CONSOLIDATION OF PRODUCTION LASER WELD PROGRAM CODE AND REDUCING FREQUENCY PARAMETERS FOR THE WELDING PROCESS.
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