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InterStim Therapy System and Verify Evaluation System (SNS Urinary)

FDA premarket approval P970004/S296 · decided 2019-08-22

Approval details

PMA number
P970004
Supplement
S296
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
InterStim Therapy System and Verify Evaluation System (SNS Urinary)
Generic name
Stimulator, electrical, implantable, for incontinence
Applicant
Medtronic Neuromodulation
Date received
2019-07-29
Decision date
2019-08-22
Days to decision
24 days
Decision code
OK30
Product code
EZW
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Minneapolis, MN
Statement
Implementation of process controls for Soft Straight-Line Finish (SLF) cosmetic rework at Medtronic’s final device manufacturing facilities-Medtronic Puerto Rico Operations Company (MPROC), located in Juncos, Puerto Rico.

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510(k) clearances by this applicant

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