FDA 510(k) Applications Submitted by Neuravi Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K173452 11/06/2017 EmboTrap ll Revascularization Device Neuravi Ltd.
K211338 05/03/2021 EMBOTRAP III Revascularization Device Neuravi Ltd.
K212908 09/13/2021 EmboTrap II Revascularization Device, EMBOTRAP III Revascularization Device Neuravi Ltd.


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