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SCS NEUROSTIMULATOR EXTERNAL/RESTOREPRIME/PRIMEADVANCED/RESTORE/RESTOREULTRA/RESTOREADVANCED/RESTORESENSOR

FDA premarket approval P840001/S200 · decided 2011-12-28

Approval details

PMA number
P840001
Supplement
S200
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
SCS NEUROSTIMULATOR EXTERNAL/RESTOREPRIME/PRIMEADVANCED/RESTORE/RESTOREULTRA/RESTOREADVANCED/RESTORESENSOR
Generic name
Stimulator, spinal-cord, totally implanted for pain relief
Applicant
Medtronic Neuromodulation
Date received
2011-12-08
Decision date
2011-12-28
Days to decision
20 days
Decision code
OK30
Product code
LGW
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
UPGRADE AND USE VERSION 6.4 OF THE HYBRID SLANT HANDLER SOFTWARE AT MEDTRONIC¿S HYBRID SUPPLIER.

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510(k) clearances by this applicant

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