HDE supplement

H050003 S012: INS FOR OBSESSIVE-COMPULSIVE DISORDER/LEAD KITS/EXTENSIONS/CONTROL MAGNET

FDA HDE supplement · 30-day notice · MEDTRONIC INC.,NEUROLOGICAL DIVISION

Key facts

Original HDE H050003
Supplement number S012
Supplement type 30-day notice
Reason for the supplement process change - manufacturer/sterilizer/packager/supplier
Trade name INS FOR OBSESSIVE-COMPULSIVE DISORDER/LEAD KITS/EXTENSIONS/CONTROL MAGNET
Generic name Stimulator, brain, implanted, for behavior modification
Applicant MEDTRONIC INC.,NEUROLOGICAL DIVISION
Product code MFR
Received date Dec 8, 2010
Decision date Jan 7, 2011

At a glance

  • No Approval order on file

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About HDE supplements

An HDE supplement asks FDA to approve a change to a Humanitarian Use Device that already holds a humanitarian device exemption.

Source: U.S. Food and Drug Administration (FDA), Humanitarian Device Exemption (HDE) database · Source date:

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