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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.
 
DeviceSynchroMed Infusion System, Ascenda Intrathecal Catheters
Generic Namepump, infusion, implanted, programmable
Applicant
MEDTRONIC Inc.
7000 central avenue ne
minneapolis, MN 55432-3576
PMA NumberP860004
Supplement NumberS375
Date Received05/28/2021
Decision Date06/25/2021
Product Code LKK 
Advisory Committee General Hospital
Supplement Type30-day notice
Supplement Reason process change - manufacturer/sterilizer/packager/supplier
Expedited Review Granted? No
Combination Product Yes
Approval Order Statement 
Newly defined and characterized solder paste inspection (SPI) process at Medtronic Tempe Campus (MTC), Medtronic’s internal supplier of hybrids used in the manufacturing of Medtronic Neuromodulation (Neuro) products.
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