Atlas FDA

MiniMed 670G System

FDA premarket approval P160017/S039 · decided 2018-04-10

Approval details

PMA number
P160017
Supplement
S039
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
2018-03-12
Decision date
2018-04-10
Days to decision
29 days
Decision code
OK30
Product code
OZP
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Northridge, CA
Statement
Adding an alternate injection molding machine and mold to produce the needle hub body component. The changes will apply to the Enlite Sensor and Guardian Sensor (3) which are part of the MiniMed 530G, MiniMed 630G, Paradigm Real-Time Revel, iPro2 CGM, and Medtronic 670G systems.

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