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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 NameRELIANCE 4-SITE
Classification Nameimplantable cardioverter defibrillator (non-crt)
Generic Nametransvenous defibrillation lead; accessory stylets
ApplicantBOSTON SCIENTIFIC-CRM
PMA NumberP910073
Supplement NumberS092
Date Received12/17/2010
Decision Date02/11/2011
Product Code
LWS[ Registered Establishments with LWS ]
Advisory Committee Cardiovascular
Supplement Typereal-time process
Supplement Reason change design/components/specifications - component
Expedited Review Granted? No
Combination Product Yes
Approval Order Statement 
Approval for a decrease in the length of the polyurethane tubing present at the proximal end of the lead and a labeling note regarding implantation technique.
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