HDE supplement
H050003 S372: Percept ™ PC BrainSense ™ Implantable Neurostimulator
FDA HDE supplement · 30-day notice · Medtronic Inc.,Neurological Division.
Key facts
| Original HDE | H050003 |
|---|---|
| Supplement number | S372 |
| Supplement type | 30-day notice |
| Reason for the supplement | process change - manufacturer/sterilizer/packager/supplier |
| Trade name | Percept ™ PC BrainSense ™ Implantable Neurostimulator |
| Generic name | Deep brain stimulator for obsessive compulsive disorder (ocd) |
| Applicant | Medtronic Inc.,Neurological Division. |
| Product code | OLM |
| Received date | Jul 23, 2026 |
| Decision date | Aug 21, 2026 |
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: