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 | SOFTWARE APPLICATION MODEL 2890 VERSION 4.10 |
Generic Name | Implantable pulse generator, pacemaker (non-CRT) |
Applicant | BOSTON SCIENTIFIC 4100 Hamline Avenue North St. Paul, MN 55112 |
PMA Number | P940031 |
Supplement Number | S028 |
Date Received | 09/08/2003 |
Decision Date | 10/31/2003 |
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 MODIFICATIONS TO THE SOFTWARE APPLICATIONS FOR THE PULSAR, PULSAR MAX, DISCOVERY, MERIDIAN, CONTAK TR, PULSAR MAX II, AND DISCOVERY II PACEMAKER SYSTEMS. |
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