|Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.|
|Generic Name||cardiac resynchronization therapy|
|Applicant|| MEDTRONIC INC.|
|Supplement Type||30-day notice|
|Supplement Reason|| process change: manufacturing|
|Expedited Review Granted?|| No|
|Approval Order Statement |
Modification of the inspection criteria for the open anode bottom (oab) and open cathode bottom (ocb) separator used in the battery of multiple implantable devices.