Atlas FDA

MiniMed 670G System

FDA premarket approval P160017/S033 · decided 2018-02-28

Approval details

PMA number
P160017
Supplement
S033
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
2018-01-29
Decision date
2018-02-28
Days to decision
30 days
Decision code
OK30
Product code
OZP
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Northridge, CA
Statement
Changes to the test method for the bolus accuracy and timing test that is performed for the insulin pump component of the Paradigm Real-time system, Paradigm Real-Time REVEL system, MiniMed 530G system, MiniMed 630G system, and MiniMed 670G 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