Atlas FDA

EMBLEM S-ICD

FDA premarket approval P110042/S157 · decided 2021-09-17

Approval details

PMA number
P110042
Supplement
S157
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
EMBLEM S-ICD
Generic name
Implantable cardioverter defibrillator (non-CRT)
Applicant
Boston Scientific Corporation
Date received
2021-06-21
Decision date
2021-09-17
Days to decision
88 days
Decision code
APPR
Product code
LWS
Advisory committee
Cardiovascular
Expedited review
No
Location
St Paul, MN
Statement
Approval for the software modifications to the LATITUDE NXT Remote Patient Management System.

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