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 | MEDTRONIC SPRINT LEADS |
Generic Name | Implantable cardioverter defibrillator (non-CRT) |
Applicant | MEDTRONIC Inc. 8200 CORAL SEA STREET NE MS MV S11 MOUNDS VIEW, MN 55112 |
PMA Number | P920015 |
Supplement Number | S038 |
Date Received | 09/12/2007 |
Decision Date | 02/06/2008 |
Product Code |
LWS |
Advisory Committee |
Cardiovascular |
Supplement Type | 135 Review Track For 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement APPROVAL FOR CHANGING THE MOLDING VENDOR AND MOLDING PROCESS PARAMETERS FOR THE IS-1 CONNECTOR SLEEVE COMPONENT FOR SPRINT LEAD MODELS 6930, 6931, 6945, 6947, 6948, 6949, AND 6944. |
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