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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.
Classification Nameimplantable cardioverter defibrillator (non-crt)
Generic Nameimplantable cardioverter defibrillator (non-crt)
4100 hamline avenue north
st. paul, MN 55112
PMA NumberP910077
Supplement NumberS084
Date Received02/28/2008
Decision Date03/17/2008
Product Code
LWS[ Registered Establishments with LWS ]
Advisory Committee Cardiovascular
Supplement Typereal-time process
Supplement Reason change design/components/specifications/material
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the latitude paceart integration (lpi) (model 6472 v1. 0) that will reside on the latitude patient management system (model 6488 v4. 0).