| 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 |
| 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 | S057 |
| Date Received | 02/11/2019 |
| Decision Date | 03/11/2019 |
| Product Code |
OZP |
| Advisory Committee |
Clinical Chemistry |
| Clinical Trials | NCT02130284
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| 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 |
| Recalls | CDRH Recalls |
Approval Order Statement Additional equipment for the production of Tyvek lid and thermoformed tray used for the packaging of Guardian (3) and Enlite sensors. The Guardian Sensor (3) is a component of of the Medtronic MiniMed 670G, MiniMed 630G with SmartGuard and Guardian Connect Systems and the Enlite Sensor is a component of the Medtronic MiniMed 530G, MiniMed 630G with SmartGuard, iPro2 and Paradigm REAL-Time Revel Systems. |
| Post-Approval Study | Show Report Schedule and Study Progress |
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