Class Class II

0.014” Willow Guidewire (K253168)

K253168 2025-11-26 Special
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Description

0.014” Willow Guidewire by Arbor Endovascular, LLC, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253168
Clearance Date2025-11-26
Clearance TypeSpecial
Product CodeMOF
Regulation Number870.1330

Categories

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