FDA 510(k)

Sistema de Fijación de Tack de Tissue Anika

N.º K: K222487 · 2023-05-08

Fecha de decisión2023-05-08

Código de productoGDW

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Anika Tissue Tack Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Anika Therapeutics, Inc.. It received FDA 510(k) clearance on 2023-05-08 under 510(k) number K222487. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Anika Tissue Tack Fixation System?

Anika Tissue Tack Fixation System is a medical device that received FDA 510(k) clearance on 2023-05-08. The listed applicant is Anika Therapeutics, Inc.. The 510(k) number is K222487.

When did Anika Tissue Tack Fixation System receive FDA 510(k) clearance?

Anika Tissue Tack Fixation System received FDA 510(k) clearance on 2023-05-08, under 510(k) number K222487.

Who is the listed applicant for Anika Tissue Tack Fixation System?

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

What is the FDA product code for Anika Tissue Tack Fixation System?

The FDA product code for Anika Tissue Tack Fixation System is GDW.

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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.