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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

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Device Name Company Date Approved Supplement Reason Other Information
interstim® therapy system, verify® evaluation system

supplement #: S410
Medtronic Neuromodulation Feb 07, 2025 process change - manufacturer/sterilizer/packager/supplier  
interstim therapy system

supplement #: S411
Medtronic Neuromodulation Dec 13, 2024 change design/components/specifications/material  
interstim therapy system, verify evaluation system

supplement #: S412
Medtronic Neuromodulation Nov 25, 2024 process change - manufacturer/sterilizer/packager/supplier  
sns urinary neurostimulator/implantable interstim

supplement #: S413
Medtronic Neuromodulation Dec 12, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim® therapy system, verify® evaluation system

supplement #: S415
Medtronic Neuromodulation Dec 05, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim therapy system, sacral nerve stimulation (sns) implantable neurostimulator

supplement #: S416
Medtronic Neuromodulation Dec 19, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim therapy system, verify evaluation system

supplement #: S417
Medtronic Neuromodulation Dec 16, 2024 process change - manufacturer/sterilizer/packager/supplier  
interstim® therapy system, verify® evaluation system

supplement #: S418
Medtronic Neuromodulation Jan 15, 2025 process change - manufacturer/sterilizer/packager/supplier  
interstim® therapy system, verify® evaluation system

supplement #: S419
Medtronic Neuromodulation Feb 28, 2025 process change - manufacturer/sterilizer/packager/supplier  
interstim® therapy system, verify® evaluation system

supplement #: S420
Medtronic Neuromodulation Mar 14, 2025 process change - manufacturer/sterilizer/packager/supplier  
  We welcome your comments and feedback about Devices@FDA.
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