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 | EVIA / ENTOVIS FAMILY OF PULSE GENERATORS |
Generic Name | Pulse generator, permanent, implantable |
Applicant | BIOTRONIK, INC. 6024 Jean Road Lake Oswego, OR 97035 |
PMA Number | P950037 |
Supplement Number | S091 |
Date Received | 12/10/2010 |
Decision Date | 03/25/2011 |
Product Code |
NVZ |
Advisory Committee |
Cardiovascular |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | No |
Review Memo | Review Memo |
Approval Order Statement APPROVAL FOR UPDATED INTEGRATED CIRCUITS FOR USE IN THE CURRENTLY MARKETED EVIA/ ENTOVIS/ESTELLA/ ECURO/EFFECTA FAMILY OF PULSE GENERATORS. |
Approval Order | Approval Order |
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