Atlas FDA

MiniMed 670G System

FDA premarket approval P160017/S044 · decided 2018-06-28

Approval details

PMA number
P160017
Supplement
S044
Supplement type
Special (Immediate Track)
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
2018-06-07
Decision date
2018-06-28
Days to decision
21 days
Decision code
APPR
Product code
OZP
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Northridge, CA
Statement
Approval for the addition of two 100% visual inspections to the needle hub assembly used in the Guardian Sensor (3) and Enlite Glucose Sensor. The Guardian Sensor (3) is a component of the MiniMed 630G System with SmartGuard, Guardian Connect System, and MiniMed 670G System. The Enlite Sensor is a component of the MiniMed 530G System, Paradigm Real-Time Revel System, MiniMed 630G System With SmartGuard, and MiniMed iPro2 CGM System with Enlite Sensor.

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510(k) clearances by this applicant

RecordFirmDate
MiniMed Flex pump (K253743)Medtronic Minimed, Inc.2026-03-12
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