| |
| Trade Name | RECLAIM DEEP BRAIN STIMULATION FOR OBSESSIVE COMPULSIVE DISORDER (OCD)THERAPY |
| Classification Name | stimulator, brain, implanted, for behavior modification |
| Generic Name | stimulator, brain, implanted, for behavior modification |
| Applicant |
| MEDTRONIC INC.,NEUROLOGICAL DIVISION |
| 7000 central avenue northeast |
| minneapolis, MN 55432 |
|
| HDE Number | H050003 |
| Supplement Number | S062 |
| Date Received | 06/06/2013 |
| Decision Date | 04/29/2016 |
| Product Code | |
| Advisory Committee |
Neurology |
| Supplement Type | normal 75 day track |
| Supplement Reason | change design/components/specifications/material |
| Expedited Review Granted? | No |
| Combination Product | No |
Approval Order Statement Approval for the replacement of the battery compartment labels of the hand-held patient programmers referenced above with labels whole pressure sensitive is resistant to the effects of high humidity. |