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 | KAINOX VCS,LINOX,LINOX SMART,VIGILA,VOLTA |
Generic Name | Permanent defibrillator electrodes |
Applicant | BIOTRONIK, INC. 6024 Jean Road Lake Oswego, OR 97035 |
PMA Number | P980023 |
Supplement Number | S055 |
Date Received | 04/29/2013 |
Decision Date | 05/29/2013 |
Product Code |
NVY |
Advisory Committee |
Cardiovascular |
Supplement Type | 30-Day Notice |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement A CHANGE IN STERILIZATION LOAD CONFIGURATION; 2) CHANGE IN STERILIZATION PRE-CONDITIONING; 3) STERILIZATION INJECTION PARAMETER CHANGES; AND 4) CHANGE TO THEPROCESS CHALLENGE DEVICE. |
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