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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.
 
DeviceProclaim DRG IPG Clinical Programmer App
Generic NameDorsal root ganglion stimulator for pain relief
ApplicantAbbott Medical
6901 Preston Road
Plano, TX 75024
PMA NumberP150004
Supplement NumberS029
Date Received03/21/2019
Decision Date09/17/2019
Product Code PMP 
Advisory Committee Neurology
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
Approval for updating the Clinician Programmer Application and Patient Controller Application to support an expanded allowable impedance range for MR Conditional devices entering MRI Mode, and to amend the labeling and software to change the term Program Mode to Dosage and Cycle to Intermittent.
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