HDE supplement

H050003 S061: RECLAIM DEEP BRAIN STIMULATION FOR OBSESSIVE COMPULSIVE DISORDER (OCD)THERAPY

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

Key facts

Original HDE H050003
Supplement number S061
Supplement type 30-day notice
Reason for the supplement process change - manufacturer/sterilizer/packager/supplier
Trade name RECLAIM DEEP BRAIN STIMULATION FOR OBSESSIVE COMPULSIVE DISORDER (OCD)THERAPY
Generic name Stimulator, brain, implanted, for behavior modification
Applicant MEDTRONIC INC.,NEUROLOGICAL DIVISION
Product code MFR
Received date May 31, 2013
Decision date Dec 11, 2013

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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