Atlas FDA

MiniMed 670G System

FDA premarket approval P160017/S052 · decided 2018-11-14

Approval details

PMA number
P160017
Supplement
S052
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
MiniMed 670G System
Generic name
Automated insulin dosing device system, single hormonal control
Applicant
Medtronic Minimed, Inc.
Date received
2018-10-15
Decision date
2018-11-14
Days to decision
30 days
Decision code
OK30
Product code
OZP
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Northridge, CA
Statement
Manufacturing facility move at one of Medtronics tier one supplier for the manual needle-hub assembly and one-press serter base component. The one-press serter is a component of the Enlite Sensor and Guardian Sensor (3). The needle-hub assembly component is used in the Medtronic Enlite Sensor and the Guardian Sensor (3). The Enlite Sensor is a component of the Medtronic MiniMed 530G, 630G with SmartGuard, Paradigm Real-Time Revel System and iPro2 Continuous Glucose Monitoring Systems and Guardia

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