OLM
- Product code
- OLM
- Device name
- Deep Brain Stimulator For Obsessive Compulsive Disorder (Ocd)
- Device class
- Class F
- Medical specialty
- Unknown
- Marketing pathway
- HDE - Humanitarian Device Exemption
- Flag
- Implant
FDA classification definition
The device is indicated for bilateral stimulation of the anterior limb of the internal capsule, this device is indicated as an adjunct to medications and as an alternative to anterior capsulotomy for treatment of chronic, severe, treatment-resistant Obsessive Compulsive Disorder (OCD) in adult patients who have failed at least three Selective Serotonin Reuptake Inhibitors (SSRIs).
Official FDA classification page: OLM
Classification and pathway per current FDA publications. Data from openFDA (CC0).