Atlas FDA

INTERSTIM II INS

FDA premarket approval P970004/S109 · decided 2011-05-06

Approval details

PMA number
P970004
Supplement
S109
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INTERSTIM II INS
Generic name
Stimulator, electrical, implantable, for incontinence
Applicant
Medtronic Neuromodulation
Date received
2011-03-16
Decision date
2011-05-06
Days to decision
51 days
Decision code
APPR
Product code
EZW
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Minneapolis, MN
Statement
ADDITION OF AN OPTIONAL DEBURRING PROCESS.

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510(k) clearances by this applicant

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