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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,
Classification Namestimulator, spinal-cord, totally implanted for pain relief
Generic Namestimulator, spinal-cord, totally implanted for pain relief
Applicant
CORDIS CORP.
po box 525700
miami, FL 33152
PMA NumberP800040
Supplement NumberS006
Date Received03/16/1984
Decision Date05/21/1984
Product Code
LGW[ Registered Establishments with LGW ]
Advisory Committee Neurology
Expedited Review Granted? No
Combination Product No
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