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Low-Profile Visualized Intraluminal Support (LVIS), LVIS Jr., LVIS EVO

FDA premarket approval P170013/S004 · decided 2022-07-28

Approval details

PMA number
P170013
Supplement
S004
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Low-Profile Visualized Intraluminal Support (LVIS), LVIS Jr., LVIS EVO
Generic name
Intracranial coil-assist stent
Applicant
MicroVention, Inc.
Date received
2021-03-12
Decision date
2022-07-28
Days to decision
503 days
Decision code
APPR
Product code
QCA
Advisory committee
Neurology
Expedited review
No
Location
Aliso Viejo, CA
Statement
Approval for the new Low-Profile Visualized Intraluminal Support (LVIS) EVO. The LVIS EVO has a modified design compared to the approved LVIS and LVIS Jr. with a change in the radiopacity profile and shorter flared ends of the stent.

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510(k) clearances by this applicant

RecordFirmDate
Wedge XL Delivery Catheter (K232542)MicroVention, Inc.2024-05-16
SOFIA EX Intracranial Support Catheter (K230775)MicroVention, Inc.2023-09-14
EmPro EPS (EP4514C-190, EP6514C-190);Nanoparasol EPS (PNP4514C-190,PNP6514C-190) (K222694)MicroVention, Inc.2023-04-27
ISAAC Neurovascular Navigation Catheter (K222115)MicroVention, Inc.2023-01-10
AZUR HydroPack 18 (45-880005; 45-880010; 45-880020; 45-880035; 45-880050; 45-880060) (K223050)MicroVention, Inc.2022-12-21
SOFIA 88 Catheter (K214024)MicroVention, Inc.2022-09-12
ERIC Retrieval Device (K211120)MicroVention, Inc.2022-03-31
BOBBY Balloon Guide Catheter (K193607)MicroVention, Inc.2020-07-21