| |
| Trade Name | Activa Dystonia Therapy System |
| Classification Name | implanted subcortical electrical stimulator (motor disorders) |
| Generic Name | implanted subcortical electrical stimulator (motor disorders) |
| Applicant |
| Medtronic Neuromodulation |
| 7000 central ave., ne, rcw225 |
| minneapolis, MN 55432 |
|
| HDE Number | H020007 |
| Supplement Number | S261 |
| Date Received | 12/10/2019 |
| Decision Date | 01/09/2020 |
| Product Code | |
| Advisory Committee |
Neurology |
| Supplement Type | 30-day notice |
| Supplement Reason | process change - manufacturer/sterilizer/packager/supplier |
| Expedited Review Granted? | No |
| Combination Product | No |
Approval Order Statement Changes to the manufacturing process (i. E. , copper plating, additional solder mask developing line) for the printed wiring board (pwb) provided from an external supplier. |