| 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 | MiniMed 670G system, MiniMed 770G system and MiniMed 780G system |
| Generic Name | Automated insulin dosing device system, single hormonal control |
| Applicant | Medtronic Minimed, Inc. 18000 Devonshire St. Northridge, CA 91325 |
| PMA Number | P160017 |
| Supplement Number | S113 |
| Date Received | 08/15/2023 |
| Decision Date | 10/30/2023 |
| Product Code |
OZP |
| Advisory Committee |
Clinical Chemistry |
| Clinical Trials | NCT02130284
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| Supplement Type | Real-Time Process |
| Supplement Reason | Change Design/Components/Specifications/Material |
| Expedited Review Granted? | No |
| Combination Product | No |
| Predetermined Change Control Plan Authorized | No |
| Recalls | CDRH Recalls |
Approval Order Statement Approval for a minor design change to the battery cap assembly component of the 630G, 670G, 770G, and 780G pumps. The 630G, 670G, 770G, and 780G pumps are a part of the MiniMed 630G system, MiniMed 670G system, MiniMed 770G system and MiniMed 780G system, respectively. |
| Post-Approval Study | Show Report Schedule and Study Progress |
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