Class Class II

EMBOTRAP III Revascularization Device (K251789)

K251789 2025-09-25 Special
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Description

EMBOTRAP III Revascularization Device by Neuravi Limited, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251789
Clearance Date2025-09-25
Clearance TypeSpecial
Product CodeNRY
Regulation Number870.1250

Categories

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