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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.
 
DeviceCORDIS PROGRAMMABLE NEURAL STIMULATOR MODELS 900A,
Generic NameStimulator, spinal-cord, totally implanted for pain relief
ApplicantCORDIS CORP.
PO BOX 525700
MIAMI, FL 33152
PMA NumberP800040
Supplement NumberS005
Date Received11/16/1983
Decision Date03/08/1984
Withdrawal Date 05/12/2016
Product Code LGW 
Advisory Committee Neurology
Expedited Review Granted? No
Combination ProductNo
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