FDA 510(k)

Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors

N.º K: K222763 · 2022-10-13

Fecha de decisión2022-10-13

Código de productoMBI

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors is the device name listed in this FDA 510(k) record. The listed applicant is Responsive Arthroscopy, LLC. It received FDA 510(k) clearance on 2022-10-13 under 510(k) number K222763. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors?

Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors is a medical device that received FDA 510(k) clearance on 2022-10-13. The listed applicant is Responsive Arthroscopy, LLC. The 510(k) number is K222763.

When did Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors receive FDA 510(k) clearance?

Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors received FDA 510(k) clearance on 2022-10-13, under 510(k) number K222763.

Who is the listed applicant for Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors?

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

What is the FDA product code for Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors?

The FDA product code for Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors is MBI.

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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.