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Restore, Itrel, Spinal Cord Stimulation Systems

FDA premarket approval P840001/S360 · decided 2017-05-23

Approval details

PMA number
P840001
Supplement
S360
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Restore, Itrel, Spinal Cord Stimulation Systems
Generic name
Stimulator, spinal-cord, totally implanted for pain relief
Applicant
Medtronic Neuromodulation
Date received
2017-04-26
Decision date
2017-05-23
Days to decision
27 days
Decision code
OK30
Product code
LGW
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
Allow the use of an additional laser welder (BATWELDLASER040 aka Sven), for the medium rate (MR) battery case-to-cover welding process at Medtronic Energy and Component Center.

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510(k) clearances by this applicant

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