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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.
 
DeviceROTAWIRE GUIDEWIRE WITH WIRECLIP TORQUER
Classification Namecatheter, coronary, atherectomy
Generic Namecatheter, coronary, atherectomy
Applicant
Boston Scientific Corp.
two scimed place
maple grove, MN 55311-1566
PMA NumberP900056
Supplement NumberS129
Date Received11/21/2013
Decision Date12/15/2013
Product Code
MCX[ Registered Establishments with MCX ]
Advisory Committee Cardiovascular
Supplement Type30-day notice
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
REMOVAL OF 34 OF THE 48 QUALITY INSPECTIONS WITHIN THE ROTAWIRE GUIDEWIRE MANUFACTURING PROCESS.
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