Premarket Approval (PMA)

Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.

• Device: Low-Profile Visualized Intraluminal Support (LVIS) and LVIS Jr.
• Generic Name: Intracranial coil-assist stent
• Applicant: MicroVention, Inc.; 35 Enterprise; Aliso Viejo, CA 92656
• PMA Number: P170013
• Supplement Number: S007
• Date Received: 09/08/2021
• Decision Date: 10/08/2021
• Product Code: QCA
• Advisory Committee: Neurology
• Supplement Type: Normal 180 Day Track No User Fee
• Supplement Reason: Postapproval Study Protocol
• Expedited Review Granted?: No
• Combination Product: No
• Predetermined Change Control Plan Authorized: No

Approval Order Statement  
Approval of the revised protocol for the post-approval study (PAS).