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MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY INCONTINENCE

FDA premarket approval P970004/S234 · decided 2017-01-18

Approval details

PMA number
P970004
Supplement
S234
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY INCONTINENCE
Generic name
Stimulator, electrical, implantable, for incontinence
Applicant
Medtronic Neuromodulation
Date received
2016-12-19
Decision date
2017-01-18
Days to decision
30 days
Decision code
OK30
Product code
EZW
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Minneapolis, MN
Statement
Transfer of manufacturing sites of the lead/stylet assembly, wire coating equipment, and pin 209563002.

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510(k) clearances by this applicant

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