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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceSpinal Cord Stimulation (SCS)
Generic NameStimulator, spinal-cord, totally implanted for pain relief
ApplicantAbbott Medical
6901 Preston Road
Plano, TX 75024
PMA NumberP010032
Supplement NumberS172
Date Received02/12/2021
Decision Date07/26/2021
Product Code LGW 
Advisory Committee Neurology
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
Approval for the replacement of the supplier for the Thermal Cutoff (TCO) component used in the lithium ion (Li-Ion) Rechargeable Battery Pack used to recharge Implanted Pulse Generator (IPG), and for a design change to the TCO component of the Battery Pack. The design change includes the addition of a bottom metal strap to the TCO component, different dimensions of the Battery Pack due to the thicker new TCO component, an increased current allowance from 2 Amps to 7 Amps, lower voltage cutoff from 32 Volts to 28 Volts, and a lower temperature cutoff of from 92C to 82C. This change is implemented to the following specific Chargers: 3720 Eon Mini LE Charger, 3722 Eon Mini LE Charging System, 3727 Eon Charger, 3726 Eon Charging System, 3730 Prodigy Charging System, 6720 Brio LE Charger, 6722 Brio LE Charging System.
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