FDA PMA

Sealant, dural

PMA Number: P240027 · 2026-09-11

ApplicantPramand, LLC

Decision Date2026-09-11

PMA NumberP240027

Product CodeNQR

Device ClassClass 3

Medical SpecialtyU

Advisory CommitteeNE

Device Summary

Sealant, dural is the device name listed in this FDA 510(k) record. The listed applicant is Pramand, LLC. It received FDA 510(k) clearance on 2026-09-11. The device is classified under product code NQR. It was reviewed by the NE advisory panel.

Frequently Asked Questions

What is the Sealant, dural?

Sealant, dural is a medical device that received FDA 510(k) clearance on 2026-09-11. The listed applicant is Pramand, LLC.

When did Sealant, dural receive FDA 510(k) clearance?

The clearance date for Sealant, dural can be found in the official FDA records.

Who is the listed applicant for Sealant, dural?

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

What is the FDA product code for Sealant, dural?

The FDA product code for Sealant, dural is NQR.

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.