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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.
 
DeviceENDOTAK C LEAD, SQ PATCH LEAD, SQ LEAD ARRAY, DSP LEAD
Generic NameImplantable cardioverter defibrillator (non-CRT)
ApplicantBOSTON SCIENTIFIC
4100 Hamline Avenue North
St. Paul, MN 55112
PMA NumberP910073
Supplement NumberS024
Date Received02/19/1998
Decision Date08/13/1998
Product Code LWS 
Advisory Committee Cardiovascular
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
Approval for a design change to provide higher pacing impedance. Teh device, as modified, will be marketed under the trade name ENDOTAK(R) Endurance(TM) Endocardial Defibrillation Lead and is indicated for use to provide pacing and rate-sensing and delivery cardioversiona nd defibrillation shocks for AICD automatic implantable cardioverter defibrillator systems.
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