• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
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
Generic Namepump, infusion, implanted, programmable
ApplicantMEDTRONIC Inc.
7000 central avenue ne
minneapolis, MN 55432-3576
PMA NumberP860004
Supplement NumberS239
Date Received10/06/2015
Decision Date11/04/2015
Product Code LKK 
Advisory Committee General Hospital
Supplement Type30-day notice
Supplement Reason process change - manufacturer/sterilizer/packager/supplier
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
APPROVAL TO RELOCATE THE SUPPLIER MANUFACTURING FACILITY FOR THE ROTOR ASSEMBLY AND THE FINISHED MOTOR COMPONENT OF THE SYNCHROMED II MOTOR APPROVED UNDER P860004/S217 AS WELL AS REPLACE EXISTING EQUIPMENT (LASER MARKING EQUIPMENT AND TOOL MAKER'S MICROSCOPE) IN THE MOTOR MANUFACTURING PROCESS.
-
-