|
Device | InterStim Therapy System and Verify Evaluation System (SNS Bowel) |
Generic Name | Implanted electrical device intended for treatment of fecal incontinence |
Regulation Number | 876.5270 |
Applicant | MEDTRONIC NEUROMODULATION 7000 CENTRAL AVENUE NE MS RCW225 MINNEAPOLIS, MN 55432 |
PMA Number | P080025 |
Supplement Number | S198 |
Date Received | 11/15/2019 |
Decision Date | 12/11/2019 |
Product Code |
QON |
Advisory Committee |
Gastroenterology/Urology |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement Update Medtronics manufacturing software, Manufacturing Execution System to Factory Works (Release 9.7), which is comprised of (1) FW Business Rule Client 9.7, (2) FW Configuration Client 9.2.2, and (3) Integrated Manufacturing Process Management (iMPM) Web Services (WS) 3.6. |