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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.
 
DeviceENDURANT STENT GRAFT SYSTEM, ENDURANT II STENT GRAFT SYSTEM, ENDURANT II AORTO-UNI-LLIAC(AUI) STENT GRAFT SYSTEM, ENDURA
Generic NameSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
ApplicantMedtronic Vascular
3576 Unocal Place
Santa Rosa, CA 95403
PMA NumberP100021
Supplement NumberS048
Date Received07/10/2015
Decision Date08/07/2015
Product Code MIH 
Advisory Committee Cardiovascular
Clinical TrialsNCT00870051
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
RecallsCDRH Recalls
Approval Order Statement  
REPLACEMENT OF THE CURRENT V-BLOCK FIXTURE AT VENTION MEDICAL WITH A NEW DELRIN FIXTURE TO FACILITATE T-TUBE SUBASSEMBLY INSPECTIONS.
Post-Approval StudyShow Report Schedule and Study Progress
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