MiniMed 530G System
FDA premarket approval P120010/S104 · decided 2017-06-23
Approval details
- PMA number
- P120010
- Supplement
- S104
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- MiniMed 530G System
- Generic name
- Automated insulin dosing , threshold suspend
- Applicant
- Medtronic, Inc.
- Date received
- 2017-05-30
- Decision date
- 2017-06-23
- Days to decision
- 24 days
- Decision code
- OK30
- Product code
- OZO
- Advisory committee
- Clinical Chemistry
- Expedited review
- No
- Location
- Northridge, CA
- Statement
- Qualification of a second injection molding machine to produce the "Hub Body" component of the Enlite Sensor (MMT-7008). The Enlite Sensor is a component of the MiniMed 530G System, the MiniMed 630G System, the Paradigm Real-Time Revel System, and the iPro2 Continuous Glucose Monitoring System.
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