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InterStim Therapy System, Verify Evaluation System; SNM Urinary Leads

FDA premarket approval P970004/S261 · decided 2018-02-06

Approval details

PMA number
P970004
Supplement
S261
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
InterStim Therapy System, Verify Evaluation System; SNM Urinary Leads
Generic name
Stimulator, electrical, implantable, for incontinence
Applicant
Medtronic Neuromodulation
Date received
2017-11-08
Decision date
2018-02-06
Days to decision
90 days
Decision code
APPR
Product code
EZW
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Minneapolis, MN
Statement
Approval for changes to the instructions for use contained in the Model 3093 Lead / Model 3889 Lead Implant Manual.

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510(k) clearances by this applicant

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