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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 II INFUSION PUMP
Generic NamePump, infusion, implanted, programmable
ApplicantMedtronic, Inc.
7000 Central Ave., NE
Minneapolis, MN 55432
PMA NumberP860004
Supplement NumberS133
Date Received06/28/2010
Decision Date08/04/2010
Product Code LKK 
Advisory Committee General Hospital
Supplement Type135 Review Track For 30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductYes
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
APPROVAL FOR INCORPORATING ADDITIONAL INSPECTIONS AND MINOR TOOLING MODIFICATIONS TO MINIMIZE THE POTENTIAL FOR THE PUMP TUBE COMPONENT TO BE DAMAGED DURING THE PUMP MANUFACTURING PROCESS OF THE SYNCHROMED II INFUSION SYSTEM, MODEL 8637.
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