Atlas FDA

37751 RECHARGE CHARGING SYSTEM

FDA premarket approval P840001/S210 · decided 2012-04-20

Approval details

PMA number
P840001
Supplement
S210
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
37751 RECHARGE CHARGING SYSTEM
Generic name
Stimulator, spinal-cord, totally implanted for pain relief
Applicant
Medtronic Neuromodulation
Date received
2012-04-04
Decision date
2012-04-20
Days to decision
16 days
Decision code
APPR
Product code
LGW
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
APPROVAL FOR LABELING CHANGES TO THE MANUALS FOR THE MODEL 37751 RECHARGE CHARGER SYSTEM, THE INFORMATION FOR PRESCRIBERS MANUAL - MEDTRONIC DBS THERAPY, AND THE INFORMATION FOR PRESCRIBERS MANUAL- MEDTRONIC PAIN THERAPY USING NEUROSTIMULATION FOR CHRONIC PAIN. THESE CHANGES INCLUDE THE ADDITION OF PRECAUTIONS RELATED TO RECHARGER USE, MODIFICATION OF THE DEVICE, AND THE EFFECT OF ELECTROMAGNETIC INTERFERENCE (EMI) ON TELEMETRY COMMUNICATION.

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