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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.
 
DeviceSELUTE PICOTIP STEROID ELUTING LEAD
Generic Namepermanent pacemaker Electrode
Regulation Number870.3680
ApplicantBoston Scientific
4100 Hamline Ave. N
St Paul, MN 55112
PMA NumberP950001
Supplement NumberS003
Date Received10/01/1997
Decision Date04/08/1998
Product Code DTB 
Advisory Committee Cardiovascular
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Approval for: a) Selute(R) Picotip(TM) Steroid Eluting, Endocardial Pacing Lead Model 4030, 4031, 4032, 4033, 4034, and 4035 which are indicated for chronic pacing and asensing of the ventricle when used with a compatible pulse generator, and b) the use of the Cosmed of Illinois facility as an alternate sterilization site.
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