|
Device | VITALITY FAMILY OF ICDS |
Generic Name | Implantable pulse generator, pacemaker (non-CRT) |
Applicant | BOSTON SCIENTIFIC 4100 Hamline Avenue North St. Paul, MN 55112 |
PMA Number | P960040 |
Supplement Number | S108 |
Date Received | 02/06/2006 |
Decision Date | 05/19/2006 |
Product Code |
LWP |
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 CHANGES TO THE TEST SOFTWARE AND TEST HARDWARE USED DURING ELECTRICAL TESTING OF THE MIXED MODE INTEGRATED CIRCUIT (MMIC). |