FDA 510(k)

Responsive Arthroscopy Interference Screw System

N.º K: K202569 · 2020-09-23

Fecha de decisión2020-09-23

Código de productoHWC

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

Responsive Arthroscopy Interference Screw System 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 2020-09-23 under 510(k) number K202569. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Responsive Arthroscopy Interference Screw System?

Responsive Arthroscopy Interference Screw System is a medical device that received FDA 510(k) clearance on 2020-09-23. The listed applicant is Responsive Arthroscopy, LLC. The 510(k) number is K202569.

When did Responsive Arthroscopy Interference Screw System receive FDA 510(k) clearance?

Responsive Arthroscopy Interference Screw System received FDA 510(k) clearance on 2020-09-23, under 510(k) number K202569.

Who is the listed applicant for Responsive Arthroscopy Interference Screw System?

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 Interference Screw System?

The FDA product code for Responsive Arthroscopy Interference Screw System is HWC. This falls under the Cardiovascular category.

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Fuente oficial

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