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 | LINOX SD, TD & S/T |
Generic Name | Implantable cardioverter defibrillator (non-CRT) |
Applicant | BIOTRONIK, INC. 6024 Jean Road Lake Oswego, OR 97035 |
PMA Number | P980023 |
Supplement Number | S030 |
Date Received | 01/07/2008 |
Decision Date | 02/29/2008 |
Product Code |
LWS |
Advisory Committee |
Cardiovascular |
Supplement Type | Real-Time Process |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | Yes |
Approval Order Statement APPROVAL FOR LEAD SUTURE SLEEVE DESIGN CHANGES, DOWNSIZED PACEMAKER SHIPPING BOXES, AND USE OF NON-LINGUAL SYMBOLS ON PACEMAKER LABELING. |
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