Atlas FDA

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

FDA premarket approval P170013/S012 · decided 2024-08-21

Approval details

PMA number
P170013
Supplement
S012
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
Low-Profile Visualized Intraluminal Support (LVIS), LVIS Jr
Generic name
Intracranial coil-assist stent
Applicant
MicroVention, Inc.
Date received
2024-03-14
Decision date
2024-08-21
Days to decision
160 days
Decision code
APPR
Product code
QCA
Advisory committee
Neurology
Expedited review
No
Location
Aliso Viejo, CA
Statement
approval of the revised protocol for the post-approval study (PAS) referenced above. The PAS protocol has been submitted to comply with the conditions of approval outlined in our approval order for P170013

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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