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. |
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Device | CONCERTO |
Applicant | MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT 8200 CORAL SEA STREET N.E. MOUNDS VIEW, MN 55112 |
PMA Number | P010031 |
Supplement Number | S093 |
Date Received | 03/04/2008 |
Decision Date | 04/03/2008 |
Advisory Committee |
Cardiovascular |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | 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. |
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