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InterStim™ Therapy System, Verify™ Evaluation System

FDA premarket approval P970004/S432 · decided 2025-08-06

Approval details

PMA number
P970004
Supplement
S432
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
2025-07-28
Decision date
2025-08-06
Days to decision
9 days
Decision code
OK30
Product code
EZW
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Minneapolis, MN
Statement
approval for an additional supplier of the oscillator 100 kHz crystal component, which provides a clock signal to the hybrid circuitry manufactured at MTC

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510(k) clearances by this applicant

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