| Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the Original HDE to get an up-to-date view of this device. |
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| 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 |
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| HDE Number | H020007 |
| Supplement Number | S228 |
| Date Received | 10/30/2018 |
| Decision Date | 11/08/2018 |
| 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 Consolidate the laser weld pull strength monitoring tests for four model families into one group (affected models: 977a160, 977a175, 977a190, 977a260, 977a275, 977a290, 977d160, 977d260, 3776, 3777, 3778, 37081, 37082, 37083, 37085, 37086). |
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