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 | CAPSUREFIX NOVUS LEAD,VITATRON CRYSTALLINE LEAD |
Generic Name | Permanent defibrillator electrodes |
Applicant | Medtronic, Inc. 8200 CORAL SEA STREET N.E. MOUNDS VIEW, MN 55112 |
PMA Number | P930039 |
Supplement Number | S094 |
Date Received | 09/30/2013 |
Decision Date | 10/17/2013 |
Product Code |
NVY |
Advisory Committee |
Cardiovascular |
Supplement Type | 30-Day Notice |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement UPDATE TO THE MANUFACTURING AND INSPECTION PROCESS FOR TUBING USED IN MEDTRONIC CRDM THERAPY DELIVERY PRODUCTS. |
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