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U.S. Department of Health and Human Services

Devices@FDA
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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.
 
DeviceMiniMed 670G System
Generic NameAutomated insulin dosing device system, single hormonal control
ApplicantMedtronic Minimed, Inc.
18000 Devonshire St.
Northridge, CA 91325
PMA NumberP160017
Supplement NumberS032
Date Received01/29/2018
Decision Date02/28/2018
Product Code OZP 
Advisory Committee Clinical Chemistry
Clinical TrialsNCT02130284
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
RecallsCDRH Recalls
Approval Order Statement  
Change of O-ring supplier for MiniMed 630G, 670G, and Paradigm REAL-Time family of insulin pumps, which are components of the MiniMed 670G System, MiniMed 630G System with SmartGuard, MiniMed Paradigm Real-Time Revel System with Enlite Sensor, MiniMed 530G System, and MiniMed Paradigm Real-Time Revel System.
Post-Approval StudyShow Report Schedule and Study Progress
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