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FDA PMA

Stent graft, bypass, superficial femoral artery

PMA Number: P220021 · 2026-01-22

ApplicantEndologix, LLC
Decision Date2026-01-22
PMA NumberP220021
Product CodeQWM
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

Stent graft, bypass, superficial femoral artery is the device name listed in this FDA 510(k) record. The listed applicant is Endologix, LLC. It received FDA 510(k) clearance on 2026-01-22. The device is classified under product code QWM. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Stent graft, bypass, superficial femoral artery?

Stent graft, bypass, superficial femoral artery is a medical device that received FDA 510(k) clearance on 2026-01-22. The listed applicant is Endologix, LLC.

When did Stent graft, bypass, superficial femoral artery receive FDA 510(k) clearance?

The clearance date for Stent graft, bypass, superficial femoral artery can be found in the official FDA records.

Who is the listed applicant for Stent graft, bypass, superficial femoral artery?

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

What is the FDA product code for Stent graft, bypass, superficial femoral artery?

The FDA product code for Stent graft, bypass, superficial femoral artery is QWM.

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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