PMA P080025S340

Device
InterStim™ Therapy System, Verify™ Evaluation System
Applicant
Medtronic Neuromodulation
PMA number
P080025
Supplement
S340
Product code
QON
Decision date
2026-02-27
Classification
Gastroenterology, Urology
Generic name
Implanted electrical device intended for treatment of fecal incontinence
Approval order statement
to implement a new Keyence Inspection System for the battery electrode compression process set-up

Current openFDA PMA Record#

Device
InterStim™ Therapy System, Verify™ Evaluation System
Applicant
Medtronic Neuromodulation
PMA number
P080025
Supplement
S340
Product code
QON
Generic name
Implanted electrical device intended for treatment of fecal incontinence
Decision date
2026-02-27
Decision code
OK30
Date received
2026-01-30
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
to implement a new Keyence Inspection System for the battery electrode compression process set-up