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MiniMed 670G System and MiniMed 770G System

FDA premarket approval P160017/S088 · decided 2020-12-01

Approval details

PMA number
P160017
Supplement
S088
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
MiniMed 670G System and MiniMed 770G System
Generic name
Automated insulin dosing device system, single hormonal control
Applicant
Medtronic Minimed, Inc.
Date received
2020-11-03
Decision date
2020-12-01
Days to decision
28 days
Decision code
OK30
Product code
OZP
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Northridge, CA
Statement
Manufacturing changes related to bioburden testing for the Enlite Sensor and Guardian Sensor (3). The Enlite Sensor is component of the MiniMed 530G System, the MiniMed 630G System, the Paradigm Real-Time Revel System, and the iPro2 CGM System. The Guardian Sensor (3) is component of the MiniMed 670G System, the Guardian Connect System, and the MiniMed 630G System with SmartGuard.

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510(k) clearances by this applicant

RecordFirmDate
MiniMed Flex pump (K253743)Medtronic Minimed, Inc.2026-03-12
MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894) (K253470)Medtronic Minimed, Inc.2026-01-15
SmartGuard technology; Predictive Low Glucose technology (K253585)Medtronic Minimed, Inc.2026-01-14
SmartGuard technology; Predictive Low Glucose technology (K251217)Medtronic Minimed, Inc.2025-08-29
MiniMed 780G insulin pump (K251032)Medtronic Minimed, Inc.2025-07-01
Extended Reservoir (K210714)Medtronic Minimed, Inc.2022-04-06
MiniMed Connect kit, MiniMed Connect uploader, MiniMed Connect app, CareLink Connect (CareLink Personal) (K151236)Medtronic Minimed, Inc.2015-05-19
MEDTRONIC MINIMED CARELINK USB CONNECTOR, MODEL NMT 7305 (K070438)Medtronic Minimed, Inc.2007-10-17