|
Device | CONTAK RENEWAL CARDIAC RESYNCHRONIZATION THERAPY DEFIBRILLATORS |
Generic Name | Implantable pulse generator, pacemaker (non-CRT) |
Applicant | Boston Scientific Corp. 4100 HAMLINE AVE NORTH ST. PAUL, MN 55112 |
PMA Number | P010012 |
Supplement Number | S121 |
Date Received | 03/27/2006 |
Decision Date | 08/09/2006 |
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 |
Recalls | CDRH Recalls |
Approval Order Statement CHANGE TO INCLUDE CIRCUIT BOARD PREPARATION TO THE CLONMEL, IRELAND FACILITY. |