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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 530G INSULIN PUMP
Generic NameAutomated insulin dosing , threshold suspend
ApplicantMedtronic, Inc.
18000 Devonshire St.
Northridge, CA 91325
PMA NumberP120010
Supplement NumberS016
Date Received03/06/2014
Decision Date06/03/2014
Product Code OZO 
Advisory Committee Clinical Chemistry
Clinical TrialsNCT01112696
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
RecallsCDRH Recalls
Approval Order Statement  
APPROVAL FOR CHANGES TO THE SOFTWARE TO THE MINIMED 530G INSULIN PUMP (MODELS MMT-551 AND MMT-751). THESE CHANGES INCLUDE CORRECTIONS FOR TWO MOTOR ERROR ANOMALIES AND THREE THRESHOLD SUSPEND ANOMALIES, AND ENHANCEMENTS FOR THE THRESHOLD SUSPEND FEATURE, INSULIN VALUE SETTING, AND MERGED COMMON CODE BASE.
Post-Approval StudyShow Report Schedule and Study Progress
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