Atlas FDA

MiniMed™ 670G System

FDA premarket approval P160017/S095 · decided 2021-12-17

Approval details

PMA number
P160017
Supplement
S095
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
2021-11-17
Decision date
2021-12-17
Days to decision
30 days
Decision code
APPR
Product code
OZP
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Northridge, CA
Statement
Approval for approval for a labeling update to provide additional clarity on an existing warning for acetaminophen interference to the continuous glucose monitoring (CGM) component of the system.

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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