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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 NumberS005
Date Received11/02/2016
Decision Date12/02/2016
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  
Move a mold to a different press and to change process parameters in the Enlite Sensor and Guardian Sensor manufacturing process. The Enlite Sensor is a component of the MiniMed-530G System, the Minimed Revel Insulin Pump System, the iPro2 CGM System, and the MiniMed 630G System. The Guardian sensor (3) is a component of the MiniMed 670G System.
Post-Approval StudyShow Report Schedule and Study Progress
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