|
Device | VENTAK PRX & VENTAK MINI I-IV |
Generic Name | Implantable cardioverter defibrillator (non-CRT) |
Applicant | BOSTON SCIENTIFIC 4100 Hamline Avenue North St. Paul, MN 55112 |
PMA Number | P910077 |
Supplement Number | S106 |
Date Received | 07/15/2010 |
Decision Date | 08/13/2010 |
Product Code |
LWS |
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 REVISION OF INSPECTION PROCEDURES FOR CERAMIC CAPACITORS, CERAMIC NETWORKS, AND CERAMIC CAPACITOR ARRAYS. |