meddevicedb.com FDA Device Reference

Vario-Cup System

K221794 Class II Special
Decision Date
2022-07-20
Sponsor / Applicant
Waldemar Link GmbH & Co. KG

Technical Specification

510(k) Submission ID K221794
Product Code KWY
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3390
Decision Date 2022-07-20
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Vario-Cup System received FDA 510(k) clearance under submission number K221794, sponsored by Waldemar Link GmbH & Co. KG. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2022-07-20.

Classification & Regulation

This clearance is catalogued under FDA product code KWY and 21 CFR 888.3390, within the Orthopedic review panel as a Class II device.