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U.S. Department of Health and Human Services

Devices@FDA
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Note: if a medical device has supplements, the device description and instructions may have
changed. Be sure to look at the supplements to get an up-to-date view of this device.
 
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438 supplements returned for P860004

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Device Name Company Date Approved Supplement Reason Other Information
synchromed infusion system

supplement #: S236
Medtronic, Inc. Dec 21, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S237
Medtronic, Inc. Oct 21, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S238
Medtronic, Inc. Oct 30, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S239
Medtronic, Inc. Nov 04, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S240
Medtronic, Inc. Nov 10, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S241
Medtronic, Inc. Nov 19, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S242
Medtronic, Inc. Nov 20, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed ii implantable infusion pump

supplement #: S243
Medtronic, Inc. Jul 22, 2016 change design/components/specifications/material  
synchromed infusion system

supplement #: S244
Medtronic, Inc. Jan 08, 2016 process change - manufacturer/sterilizer/packager/supplier  
synchromed ii pump

supplement #: S245
Medtronic, Inc. Feb 18, 2016 process change - manufacturer/sterilizer/packager/supplier  
  We welcome your comments and feedback about Devices@FDA.
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