| 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 | S077 |
| Date Received | 11/09/2015 |
| Decision Date | 12/09/2015 |
| Product Code |
OZO |
| Advisory Committee |
Clinical Chemistry |
| Clinical Trials | NCT01112696
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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 TO MAKE CHANGES IN THE INCOMING INSPECTION CRITERIA FOR THE BLUE TEST PLUG TO REMOVE THE INSPECTION OF 5 NON-CRITICAL DIMENSIONS. THE BLUE TEST PLUG IS INTENDED FOR USE WITH THE MINILINK TRANSMITTER (MMT-7703) AND IT IS AN ACCESSORY OF PARADIGM REAL-TIME, PARADIGM REAL-TIME REVEL, AND MINIMED 530G SYSTEMS. |
| Post-Approval Study | Show Report Schedule and Study Progress |
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