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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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435 supplements returned for P970004

New Search  Back to Search Results | Help
Device Name Company Date Approved Supplement Reason Other Information
interstim® therapy system, verify® evaluation system

supplement #: S400
Medtronic Neuromodulation May 23, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim® therapy system, verify® evaluation system

supplement #: S401
Medtronic Neuromodulation Jun 28, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim therapy system, verify evaluation system

supplement #: S402
Medtronic Neuromodulation Jul 05, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim therapy system, verify® evaluation system

supplement #: S403
Medtronic Neuromodulation Aug 14, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim® therapy system, verify® evaluation system

supplement #: S404
Medtronic Neuromodulation Jul 29, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim therapy system

supplement #: S405
Medtronic Neuromodulation Sep 16, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim therapy system, verify evaluation system

supplement #: S406
Medtronic Neuromodulation Sep 30, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim® therapy system

supplement #: S407
Medtronic Neuromodulation Oct 11, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim therapy system, verify evaluation system

supplement #: S408
Medtronic Neuromodulation Feb 12, 2025 process change - manufacturer/sterilizer/packager/supplier  
interstim therapy system, verify evaluation system

supplement #: S409
Medtronic Neuromodulation Jan 06, 2025 change design/components/specifications/material  
  We welcome your comments and feedback about Devices@FDA.
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