Willow 18 Guidewire
K-Number: K260130 · 2026-02-13
ApplicantArbor Endovascular, LLC
Decision Date2026-02-13
Product CodeMOF
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Willow 18 Guidewire is a medical device manufactured by Arbor Endovascular, LLC. It received FDA 510(k) clearance on 2026-02-13 under approval number K260130. The device is classified under product code MOF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Willow 18 Guidewire?
Willow 18 Guidewire is a medical device that received FDA 510(k) clearance on 2026-02-13. It is manufactured by Arbor Endovascular, LLC. The 510(k) number is K260130.
When was Willow 18 Guidewire approved by the FDA?
Willow 18 Guidewire received FDA 510(k) clearance on 2026-02-13, under approval number K260130.
What company makes Willow 18 Guidewire?
Willow 18 Guidewire is manufactured by Arbor Endovascular, LLC.
What is the FDA product code for Willow 18 Guidewire?
The FDA product code for Willow 18 Guidewire is MOF.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.