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MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL

FDA premarket approval P970004/S211 · decided 2016-03-31

Approval details

PMA number
P970004
Supplement
S211
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL
Generic name
Stimulator, electrical, implantable, for incontinence
Applicant
Medtronic Neuromodulation
Date received
2016-03-04
Decision date
2016-03-31
Days to decision
27 days
Decision code
OK30
Product code
EZW
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Minneapolis, MN
Statement
Assembly of hybrid assemblies manufactured at Medtronic Tempe Campus using the Assembleon Pick and Place machine.

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510(k) clearances by this applicant

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