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U.S. Department of Health and Human Services

Devices@FDA
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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.
 
DeviceASCENDA INTRATHECAL CATHETER
Generic NamePump, infusion, implanted, programmable
ApplicantMedtronic, Inc.
7000 Central Ave., NE
Minneapolis, MN 55432
PMA NumberP860004
Supplement NumberS175
Date Received08/28/2012
Decision Date01/07/2013
Product Code LKK 
Advisory Committee General Hospital
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
RecallsCDRH Recalls
Approval Order Statement  
APPROVAL FOR A MINOR DESIGN CONTROL CHANGE, AND SUBSEQUENT MANUFACTURING PROCESS CHANGES, TO REMOVE THE LACK OF LAMINATION NOTE FROM THE PUMP AND SPINAL CATHETER SEGMENTS ASSEMBLY LEVEL PRINTS FOR THE DEVICE.
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