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 | VENTAK(R) PRIZM(TM) DR/VR HE SYSTEM |
Generic Name | Implantable pulse generator, pacemaker (non-CRT) |
Applicant | BOSTON SCIENTIFIC 4100 Hamline Avenue North St. Paul, MN 55112 |
PMA Number | P960040 |
Supplement Number | S016 |
Date Received | 06/29/2000 |
Decision Date | 08/07/2000 |
Product Codes |
KRG LWP |
Advisory Committee |
Cardiovascular |
Supplement Type | Real-Time Process |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement APPROVAL FOR THE HIGH ENERGY AUTOMATIC IMPLANTABLE CARDIOVASCULAR DEFIBRILLATOR (AICD) SYSTEM, MODELS 1852, 1853, 1857, AND 1858. |
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