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U.S. Department of Health and Human Services

Devices@FDA
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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.
 
DeviceGUIDANT CONTAK RENEWAL TR MODELS H125 AND H120
Generic Namepermanent pacemaker Electrode
Regulation Number870.3680
ApplicantGuidant Corp.
4100 Hamline Ave. N
St Paul, MN 55112
PMA NumberP030005
Supplement NumberS005
Date Received11/22/2004
Decision Date03/08/2005
Product Code DTB 
Advisory Committee Cardiovascular
Supplement TypeNormal 180 Day Track
Supplement Reason Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
RecallsCDRH Recalls
Approval Order Statement  
APPROVAL FOR MODIFIED DEVICE LABELING TO DESCRIBE THE COMPANION CLINICAL STUDY.
  We welcome your comments and feedback about Devices@FDA.
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