Atlas FDA

InterStim Therapy System, Verify Evaluation System

FDA premarket approval P970004/S398 · decided 2024-04-24

Approval details

PMA number
P970004
Supplement
S398
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
InterStim Therapy System, Verify Evaluation System
Generic name
Stimulator, electrical, implantable, for incontinence
Applicant
Medtronic Neuromodulation
Date received
2024-04-11
Decision date
2024-04-24
Days to decision
13 days
Decision code
OK30
Product code
EZW
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Minneapolis, MN
Statement
to implement a rework process for the Nitric Acid cleaning process

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510(k) clearances by this applicant

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