Atlas FDA

InterStim Therapy System SNS Bowel

FDA premarket approval P080025/S171 · decided 2018-08-14

Approval details

PMA number
P080025
Supplement
S171
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
InterStim Therapy System SNS Bowel
Generic name
Implanted electrical device intended for treatment of fecal incontinence
Applicant
Medtronic Neuromodulation
Date received
2018-07-17
Decision date
2018-08-14
Days to decision
28 days
Decision code
OK30
Product code
QON
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Minneapolis, MN
Statement
Alternate manufacturing site to perform the parts passivation / nitric acid cleaning for piece parts (components).

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510(k) clearances by this applicant

RecordFirmDate
SureTune4 Software (DEN210003)Medtronic Neuromodulation2021-08-23