meddevicedb.com FDA Device Reference

Active-V Total Knee System; World Total Knee System

K253239 Class II Traditional
Decision Date
2025-12-23
Sponsor / Applicant
Signature Orthopaedics Pty, Ltd.

Technical Specification

510(k) Submission ID K253239
Product Code MBH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3565
Decision Date 2025-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Active-V Total Knee System; World Total Knee System received FDA 510(k) clearance under submission number K253239, 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 2025-12-23.

Classification & Regulation

This clearance is catalogued under FDA product code MBH and 21 CFR 888.3565, within the Orthopedic review panel as a Class II device.