meddevicedb.com FDA Device Reference

CD HORIZON SPINAL SYSTEM

K082236 Class II Special
Decision Date
2008-10-10
Sponsor / Applicant
Medtronic Sofamor Danek

Technical Specification

510(k) Submission ID K082236
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2008-10-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CD HORIZON SPINAL SYSTEM received FDA 510(k) clearance under submission number K082236, 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 2008-10-10.

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.