| 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 iPro2 CGM System with Enlite Sensor |
| Generic Name | Sensor, glucose, invasive |
| Applicant | Medtronic Minimed 18000 Devonshire St. Northridge, CA 91325 |
| PMA Number | P150029 |
| Supplement Number | S013 |
| Date Received | 11/24/2017 |
| Decision Date | 12/21/2017 |
| Product Codes |
MDS OZO |
| Advisory Committee |
Clinical Chemistry |
| 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 Addition of a new sterilization site for the Enlite Sensor and the Guardian Sensor (3). The Enlite Sensor is a component of MiniMed 530G System, MiniMed Paradigm Real-Time Revel System, and MiniMed iPro2 CGM System with Enlite Sensor. The Guardian Sensor (3) is a component of MiniMed 630G System with SmartGuard and the MiniMed 670G System. |
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