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FDA PMA

Stent graft, infrapopliteal, venous arterialization

PMA Number: P220025 · 2026-01-07

ApplicantLimFlow, Inc.
Decision Date2026-01-07
PMA NumberP220025
Product CodeQWN
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

Stent graft, infrapopliteal, venous arterialization is the device name listed in this FDA 510(k) record. The listed applicant is LimFlow, Inc.. It received FDA 510(k) clearance on 2026-01-07. The device is classified under product code QWN. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Stent graft, infrapopliteal, venous arterialization?

Stent graft, infrapopliteal, venous arterialization is a medical device that received FDA 510(k) clearance on 2026-01-07. The listed applicant is LimFlow, Inc..

When did Stent graft, infrapopliteal, venous arterialization receive FDA 510(k) clearance?

The clearance date for Stent graft, infrapopliteal, venous arterialization can be found in the official FDA records.

Who is the listed applicant for Stent graft, infrapopliteal, venous arterialization?

The FDA 510(k) record lists LimFlow, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stent graft, infrapopliteal, venous arterialization?

The FDA product code for Stent graft, infrapopliteal, venous arterialization is QWN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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