|
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 avenue ne |
rcw 225 |
minneapolis, MN 55432 |
|
HDE Number | H020007 |
Supplement Number | S269 |
Date Received | 04/09/2020 |
Decision Date | 05/08/2020 |
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 Change requested to modify the procedure for the assessment of device bioburden at medtronic's final device manufacturing facilities-medtronic puerto rico operations company, located in juncos, puerto rico. The change also requested other related administrative changes which update the procedure. |