Atlas FDA

Merlin.net™ MN5000

FDA premarket approval P030054/S418 · decided 2024-10-11

Approval details

PMA number
P030054
Supplement
S418
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Merlin.net™ MN5000
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Applicant
ABBOTT MEDICAL
Date received
2024-02-13
Decision date
2024-10-11
Days to decision
241 days
Decision code
APPR
Product code
NIK
Advisory committee
Cardiovascular
Expedited review
No
Location
Sylmar, CA
Statement
Approval for the AVEIR™ Remote Care System designed to provide remote monitoring support for patients implanted with an Aveir Leadless Pacemaker(s).

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