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FDA PMA

Glue, surgical, arteries

PMA Number: P010003 · 2026-07-15

ApplicantCryolife, Inc.
Decision Date2026-07-15
PMA NumberP010003
Product CodeMUQ
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

Glue, surgical, arteries is the device name listed in this FDA 510(k) record. The listed applicant is Cryolife, Inc.. It received FDA 510(k) clearance on 2026-07-15. The device is classified under product code MUQ. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Glue, surgical, arteries?

Glue, surgical, arteries is a medical device that received FDA 510(k) clearance on 2026-07-15. The listed applicant is Cryolife, Inc..

When did Glue, surgical, arteries receive FDA 510(k) clearance?

The clearance date for Glue, surgical, arteries can be found in the official FDA records.

Who is the listed applicant for Glue, surgical, arteries?

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

What is the FDA product code for Glue, surgical, arteries?

The FDA product code for Glue, surgical, arteries is MUQ.

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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