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InterStim Therapy System and Verify Evaluation System

FDA premarket approval P970004/S299 · decided 2019-11-26

Approval details

PMA number
P970004
Supplement
S299
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
InterStim Therapy System and Verify Evaluation System
Generic name
Stimulator, electrical, implantable, for incontinence
Applicant
Medtronic Neuromodulation
Date received
2019-08-30
Decision date
2019-11-26
Days to decision
88 days
Decision code
APPR
Product code
EZW
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Minneapolis, MN
Statement
Approval for an update to the inner packaging tray that holds the torque wrench.

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510(k) clearances by this applicant

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