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WEB Aneurysm Embolization System

Microvention, Inc. · Model W4-4-3-MVI-3 · UDI-DI 00842429106969

OPR Prescription
0
510(k) clearances
889
Adverse events (34 deaths)
1
Recalls
7
Facilities

Description

WEB 21 SL 4x3

Recalls

DateFirmReason
2022-09-21MICROVENTION INC.Detachment controller, of an aneurysm embolization system, has an out of specification tunnel opening dimension, which may prevent the implant device pusher from being fully insert

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.