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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 NameEXPRESS LD LLIAC PREMOUNTED STENT SYSTEM
Classification Namestent, iliac
ApplicantBOSTON SCIENTIFIC CORPORATION
PMA NumberP090003
Supplement NumberS001
Date Received04/15/2010
Decision Date05/13/2010
Product Code
NIO[ Registered Establishments with NIO ]
Advisory Committee Cardiovascular
Supplement Type30-day notice
Supplement Reason process change: manufacturing
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Change to the software used during a step in the stent manufacturing process.
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