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EXPEDIUM SPINE SYSTEM

K073126 Class II Special
Decision Date
2007-12-06
Sponsor / Applicant
Depuy Spine, Inc.

Technical Specification

510(k) Submission ID K073126
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2007-12-06
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 K073126, 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 2007-12-06.

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.