meddevicedb.com FDA Device Reference

World Total Knee System

K181530 Class II Traditional
Decision Date
2018-10-24
Sponsor / Applicant
Signature Orthopaedics Pty, Ltd.

Technical Specification

510(k) Submission ID K181530
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2018-10-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

World Total Knee System received FDA 510(k) clearance under submission number K181530, sponsored by Signature Orthopaedics Pty, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2018-10-24.

Classification & Regulation

This clearance is catalogued under FDA product code JWH and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.