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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.
 
DeviceLiberta RC™ DBS IPG
Generic NameStimulator, electrical, implanted, for parkinsonian tremor
ApplicantAbbott Medical
6901 Prestion Road
Plano, TX 75024
PMA NumberP140009
Supplement NumberS092
Date Received02/05/2024
Decision Date05/02/2024
Product Codes MHY NHL PJS 
Advisory Committee Neurology
Supplement TypeReal-Time Process
Supplement Reason Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
approval for the standardization of the presentation of dimensions of the Liberta RC DBS IPG (model 62400) and the Eterna SCS IPG (model 32400) within device labeling, basing them on nominal specification values via a computer-generated engineering model
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