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Low-Profile Visualized Intraluminal Support (LVIS) and LVIS Jr.

FDA premarket approval P170013 · decided 2018-05-30

Approval details

PMA number
P170013
Trade name
Low-Profile Visualized Intraluminal Support (LVIS) and LVIS Jr.
Generic name
Intracranial coil-assist stent
Applicant
MicroVention, Inc.
Date received
2017-03-31
Decision date
2018-05-30
Days to decision
425 days
Decision code
APPR
Product code
QCA
Advisory committee
Neurology
Expedited review
No
Location
Aliso Viejo, CA
Statement
Approval for the Low-Profile Visualized Intraluminal Support (LVIS) and LVIS Jr. This device is indicated for use with neurovascular embolization coils in patients >= 18 years of age for the treatment of wide-neck (neck width >= 4 mm or dome to neck ratio < 2) saccular intracranial aneurysms arising from a parent vessel with a diameter >= 2.0 mm and <= 4.5 mm.

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