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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.
 
DevicePROMETRA PROGRAMMABLE PUMP SYSTEM
Generic NamePump, infusion, implanted, programmable
ApplicantInfusyn Therapeutics, LLC
121 Shelley Dr.
2h
Hackettstown, NJ 07840
PMA NumberP080012
Supplement NumberS031
Date Received10/20/2015
Decision Date12/28/2015
Product Code LKK 
Advisory Committee General Hospital
Supplement TypeNormal 180 Day Track No User Fee
Supplement Reason Postapproval Study Protocol - OSB
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
APPROVAL OF THE FOLLOWING CHANGES TO THE POST-APPROVAL STUDY FOR THE DEVICE: A REVISION TO ALLOW FOR THE USE OF THE APPROVED PATIENT THERAPY CONTROLLER OR PTC IN THE POST-APPROVAL CLINICAL STUDY FOR THE PROMETRA IMPLANTABLE PROGRAMMABLE PUMP SYSTEM.
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