meddevicedb.com FDA Device Reference

CD HORIZON SPIRE Z SPINAL SYSTEM

K123246 Class II Special
Decision Date
2012-11-16
Sponsor / Applicant
Medtronic Sofamor Danek

Technical Specification

510(k) Submission ID K123246
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2012-11-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CD HORIZON SPIRE Z SPINAL SYSTEM received FDA 510(k) clearance under submission number K123246, sponsored by Medtronic Sofamor Danek. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-11-16.

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.