Atlas FDA

SYNERGY/SYNERGY VERSITREL IPS/RESTOREPRIME IMPLANTABLE NEUROSTIMULATOR/PRIMEADVANCED/RESTORE/RESTOREULTRA/RESTOREADVANCE

FDA premarket approval P840001/S182 · decided 2011-05-06

Approval details

PMA number
P840001
Supplement
S182
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
SYNERGY/SYNERGY VERSITREL IPS/RESTOREPRIME IMPLANTABLE NEUROSTIMULATOR/PRIMEADVANCED/RESTORE/RESTOREULTRA/RESTOREADVANCE
Generic name
Stimulator, spinal-cord, totally implanted for pain relief
Applicant
Medtronic Neuromodulation
Date received
2011-03-16
Decision date
2011-05-06
Days to decision
51 days
Decision code
APPR
Product code
LGW
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
ADDITION OF AN OPTIONAL DEBURRING PROCESS.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

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