| 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 | SOF-SENSOR |
| Generic Name | Sensor, glucose, invasive |
| Applicant | Medtronic Minimed 18000 Devonshire St. Northridge, CA 91325 |
| PMA Number | P980022 |
| Supplement Number | S167 |
| Date Received | 10/31/2014 |
| Decision Date | 01/29/2015 |
| Product Code |
MDS |
| Advisory Committee |
Clinical Chemistry |
| 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 |
Approval Order Statement APPROVAL FOR USE OF A THICKER DOUBLE-SIDED TAPE ON THE SOF-SENSOR (MODEL MMT-7002, MMT-7003 AND ENLITE SENSOR (MMT-7008) BASE AS WELL AS CHANGE IN THECONVERTER/DISTRIBUTOR OF THE TAPE. THE SOF-SENSOR (MODEL MMT-7002, MMT-7003) IS A COMPONENT OF THE PARADIGM REAL-TIME, PARADIGM REAL-TIME REVEL, GUARDIAN REAL-TIME, MINILINK REAL-TIME, AND IPRO2 PROFESSIONAL CGM SYSTEMS AND THE ENLITE GLUCOSE SENSOR (MMT-7008) IS A COMPONENT OF THE MINIMED 530G SYSTEM. |
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