| 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 | SYNERGYST II PULSE GENERATOR MODELS 7070 & 7071 |
| Generic Name | Pulse generator, permanent, implantable |
| Applicant | Medtronic, Inc. 8200 Coral Sea St. N.E Mounds View, MN 55112 |
| PMA Number | P890003 |
| Supplement Number | S481 |
| Date Received | 07/10/2025 |
| Decision Date | 10/30/2025 |
| Product Code |
NVZ |
| Advisory Committee |
Cardiovascular |
| Supplement Type | Normal 180 Day Track No User Fee |
| Supplement Reason | Labeling Change - PAS |
| Expedited Review Granted? | No |
| Combination Product | No |
| Predetermined Change Control Plan Authorized | No |
Approval Order Statement Approval for updated labeling to include results from the post approval study (PAS) Heart Failure Risk Status (HFRS) PAS, as summarized in the final report P890003/R098. |
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