|
Device | Drug-Eluting Permanent Defibrillator Electrodes |
Generic Name | Implantable cardioverter defibrillator (non-CRT) |
Applicant | BIOTRONIK, INC. 6024 Jean Road Lake Oswego, OR 97035 |
PMA Number | P980023 |
Supplement Number | S117 |
Date Received | 11/23/2022 |
Decision Date | 12/16/2022 |
Product Code |
LWS |
Advisory Committee |
Cardiovascular |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement Modify the process monitoring select ICD lead families to increase efficiency in the lead manufacturing process. |