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InterStim™ Therapy System, Verify™ Evaluation System

FDA premarket approval P970004/S397 · decided 2024-06-11

Approval details

PMA number
P970004
Supplement
S397
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
InterStim™ Therapy System, Verify™ Evaluation System
Generic name
Stimulator, electrical, implantable, for incontinence
Applicant
Medtronic Neuromodulation
Date received
2024-03-19
Decision date
2024-06-11
Days to decision
84 days
Decision code
APPR
Product code
EZW
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Minneapolis, MN
Statement
a minor change to the inner tray used for percutaneous extension kits

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510(k) clearances by this applicant

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