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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 supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameSELUTE(R) STEROID-ELUTING LEAD
Classification Namepermanent pacemaker electrode
Generic Namealternate endocardial lead stabilizer component
Regulation Number870.3680
ApplicantGUIDANT CORP.
PMA NumberP950001
Supplement NumberS005
Date Received12/16/1999
Decision Date03/10/2000
Product Code
DTB[ Registered Establishments with DTB ]
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - component
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval is for the use of a modified suture sleeve.
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