Atlas FDA

MiniMed 670G System, MiniMed 770G System

FDA premarket approval P160017/S089 · decided 2021-04-19

Approval details

PMA number
P160017
Supplement
S089
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
MiniMed 670G System, MiniMed 770G System
Generic name
Automated insulin dosing device system, single hormonal control
Applicant
Medtronic Minimed, Inc.
Date received
2020-12-17
Decision date
2021-04-19
Days to decision
123 days
Decision code
APPR
Product code
OZP
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Northridge, CA
Statement
Approval to introduce the MiniMed 770G System to the post-approval study and to provide protocol updates to meet enrollment requirements.

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510(k) clearances by this applicant

RecordFirmDate
MiniMed Flex pump (K253743)Medtronic Minimed, Inc.2026-03-12
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