Atlas FDA

Quartet™

FDA premarket approval P030054/S424 · decided 2024-09-26

Approval details

PMA number
P030054
Supplement
S424
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Quartet™
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Applicant
ABBOTT MEDICAL
Date received
2024-06-28
Decision date
2024-09-26
Days to decision
90 days
Decision code
APPR
Product code
NIK
Advisory committee
Cardiovascular
Expedited review
No
Location
Sylmar, CA
Statement
approval for expanding MR Conditional labeling for Quadra Allure and Allure MP Cardiac Resynchronization Therapy Pacemaker (CRT-P) systems with Tendril STS, UltiPace, Quartet, and IsoFlex pacing leads.

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