| Device |
percutaneous nerve stimulator for opioid withdrawal |
| Regulation Description |
Percutaneous nerve stimulator for substance use disorders. |
| Definition |
Stimulate nerve branches to aid in the reduction of symptoms associated with substance use disorders. |
| Physical State |
A signal generator connected to percutaneous electrodes. |
| Technical Method |
Electrical stimulation of nerve branches using percutaneous electrodes. |
| Target Area |
Cranial and occipital nerve branches. |
| Regulation Medical Specialty |
Neurology |
| Review Panel |
Neurology |
| Product Code | PZR |
| Premarket Review |
Neuromodulation and Physical Medicine Devices
(DHT5B)
Neuromodulation and Physical Medicine Devices
(DHT5B)
|
| Submission Type |
510(k)
|
| Regulation Number |
882.5896
|
| Device Class |
2
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
Summary Malfunction Reporting |
Ineligible |
| Implanted Device? |
No
|
| Life-Sustain/Support Device? |
No
|
| Third Party Review |
Not Third Party Eligible |