FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Automated Insulin Dosing Device System, Single Hormonal Control
PMA: P160017
·
Supplement: S086
·
Decision Sep 2, 2020
Classifications
1
FEI Numbers
16
Registration Numbers
16
Basic Information
- Device Name
- Automated Insulin Dosing Device System, Single Hormonal Control
- Trade Name
- MiniMed 670G System
- PMA Number
- P160017
- Supplement Number
- S086
- 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
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- September 2, 2020
- Date Received
- August 4, 2020
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
IntriCon Corporation (IntriCon Red Fox), 1260 Red Fox Road, Saint Paul, MN as an alternative finished product manufacturing facility and IntriCon Corporation Grey Fox (IntriCon Grey Fox), 1275 Grey Fox Road Arden Hills, MN as an alternate final packaging process facility for the Guardian Link (3) and Guardian Connect Transmitter. The transmitters are components of the MiniMed 630G System with SmartGuard, Guardian Connect System, and MiniMed 670G System. The submission also requested approval of process changes related to the new manufacturing facilities including a new inspection process and equipment.
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 |