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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.
 
DeviceAFX ENDOVASCULAR AAA SYSTEM
Generic NameSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
ApplicantEndologix, LLC
2 Musick
Irvine, CA 92618
PMA NumberP040002
Supplement NumberS040
Date Received11/08/2012
Decision Date12/28/2012
Product Code MIH 
Advisory Committee Cardiovascular
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
APPROVAL FOR THE ADDITION OF BIFURCATED STENT GRAFT MODELS FOR THE APPROVED AFX ENDOVASCULAR AAA SYSTEM PRODUCT FAMILY. THE NEW MODELS CONTAIN SHORTER AND LONGER BIFURCATED BODIES THAT WILL HAVE THE SAME DIAMETER AS THOSE CURRENTLY APPROVED; AND TO ADD 20MM DIAMETER LIMBS USING THE SAME STENT CAGE.
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