meddevicedb.com FDA Device Reference

EXPEDIUM SPINE SYSTEM

K051024 Class II Special
Decision Date
2005-07-06
Sponsor / Applicant
Depuy Spine, Inc.

Technical Specification

510(k) Submission ID K051024
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2005-07-06
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXPEDIUM SPINE SYSTEM received FDA 510(k) clearance under submission number K051024, sponsored by Depuy Spine, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2005-07-06.

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.