PMA de la FDA

Sealant, dural

Número de PMA: P220014 · 2026-08-05

SolicitantePramand, LLC

Fecha de decisión2026-08-05

Número PMAP220014

Código de productoNQR

Clase del dispositivoClase 3

Especialidad médicaU

Comité asesorNE

Resumen del dispositivo

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 2026-08-05. The device is classified under product code NQR. It was reviewed by the NE advisory panel.

Preguntas frecuentes

What is the Sealant, dural?

Sealant, dural is a medical device that received FDA 510(k) clearance on 2026-08-05. 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.

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.