meddevicedb.com FDA Device Reference

C-Zero Pedicle Screw System, Freedom Pedicle Screw System

K180754 Class II Traditional
Decision Date
2018-12-07
Sponsor / Applicant
Signature Orthopaedics Pty, Ltd.

Technical Specification

510(k) Submission ID K180754
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2018-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

C-Zero Pedicle Screw System, Freedom Pedicle Screw System received FDA 510(k) clearance under submission number K180754, 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 2018-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.