FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Automated Insulin Dosing Device System, Single Hormonal Control
PMA: P160017
·
Supplement: S123
·
Decision May 9, 2025
Classifications
1
FEI Numbers
16
Registration Numbers
16
Basic Information
- Device Name
- Automated Insulin Dosing Device System, Single Hormonal Control
- Trade Name
- MiniMed 770G Insulin Pump; MiniMed 780G Insulin Pump
- PMA Number
- P160017
- Supplement Number
- S123
- Device Class
- FDA Class 3
- Product Code
- OZP
- Generic Name
- Automated insulin dosing device system, single hormonal control
- Medical Specialty
- Unknown
- Advisory Committee
- Clinical Chemistry
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- May 9, 2025
- Date Received
- March 24, 2025
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
approval for minor design changes to the pump case of the MiniMed 770G and 780G insulin pumps. The proposed changes address failure modes in connection with recall number Z-0003-2025
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| OZP | Automated Insulin Dosing Device System, Single Hormonal Control | FDA class 3 | Unknown |