| 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 | Percepta Bipolar and Quadripolar CRT-P, Serena Bipolar and Quadripolar CRT-P, Solar Bipolar and Quadripolar CRT-P |
| Generic Name | Implantable pulse generator, pacemaker (non-CRT) |
| Applicant | Medtronic, Inc. 8200 Coral Sea St. N.E Ms Mvs11 Mounds View, MN 55112 |
| PMA Number | P010015 |
| Supplement Number | S413 |
| Date Received | 06/20/2019 |
| Decision Date | 07/18/2019 |
| Product Code |
LWP |
| Advisory Committee |
Cardiovascular |
| Supplement Type | 30-Day Notice |
| Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Expedited Review Granted? | No |
| Combination Product | No |
| Predetermined Change Control Plan Authorized | No |
Approval Order Statement Update the Parallel Gap Welding (PGW) equipment controller, the test method to detect weak welds, and to leverage the PGW process to standardize work. |
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