| 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 530G SYSTEM |
| Generic Name | Automated insulin dosing , threshold suspend |
| Applicant | Medtronic, Inc. 18000 Devonshire St. Northridge, CA 91325 |
| PMA Number | P120010 |
| Supplement Number | S062 |
| Date Received | 02/18/2015 |
| Decision Date | 05/19/2015 |
| Product Code |
OZO |
| Advisory Committee |
Clinical Chemistry |
| Clinical Trials | NCT01112696
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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 CHANGE TO THE SHELF HEIGHT DIMENSIONS OF THE WATERTIGHT TESTER (MMT-7726), A COMPONENT OF THE MINILINK REAL-TIME CONTINUOUS GLUCOSE MONITORING SYSTEM AND THE MINIMED 530G SYSTEM. |
| Post-Approval Study | Show Report Schedule and Study Progress |
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