meddevicedb.com FDA Device Reference

EXPEDIUM SPINE SYSTEM

K130877 Class II Traditional
Decision Date
2013-06-20
Sponsor / Applicant
Medos International SARL

Technical Specification

510(k) Submission ID K130877
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2013-06-20
Clearance Pathway Traditional

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 K130877, sponsored by Medos International SARL. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-06-20.

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.