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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 NameANGIOSCULPT SCORING BALLOON CATHETER
Classification Namecatheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring
Generic Namepercutaneous transluminal coronary angioplasty catheter
ApplicantANGIOSCORE INC
PMA NumberP050018
Supplement NumberS003
Date Received05/30/2007
Decision Date10/18/2007
Product Code
NWX[ Registered Establishments with NWX ]
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track no user fee
Supplement Reason location change: manufacturer
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for a manufacturing site located at angioscore, inc. , fremont, california.
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