Atlas FDA

MiniMed 670G System

FDA premarket approval P160017/S129 · decided 2025-10-02

Approval details

PMA number
P160017
Supplement
S129
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
MiniMed 670G System
Generic name
Automated insulin dosing device system, single hormonal control
Applicant
Medtronic Minimed, Inc.
Date received
2025-09-04
Decision date
2025-10-02
Days to decision
28 days
Decision code
APPR
Product code
OZP
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Northridge, CA
Statement
Approval for changes to the labeling to include formatting changes and new warnings for battery depletion, delivery volume accuracy during air travel, and pump to infusion set distance.

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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