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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.
 
DeviceFRONTIER & FRONTIER II PACEMAKERS
Generic NamePulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
ApplicantABBOTT MEDICAL
15900 Valley View Ct.
Sylmar, CA 91335
PMA NumberP030035
Supplement NumberS015
Date Received05/15/2006
Decision Date06/08/2006
Product Code NKE 
Advisory Committee Cardiovascular
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
CHANGE FROM A MANUAL TO AN AUTOMATED PROCESS TO REMOVE HYDROHONE BEADS AND AIR DRY THE PACEMAKERS FOLLOWING THIS HYDROHONING PROCESS, WHICH WILL BE PERFORMED USING THE CYCLONE WASH-DRY MACHINE.
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