meddevicedb.com FDA Device Reference

INDEPENDENCE® Spacers

K170157 Class II Traditional
Decision Date
2017-09-25
Sponsor / Applicant
Globus Medical, Inc.

Technical Specification

510(k) Submission ID K170157
Product Code OVD
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2017-09-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INDEPENDENCE® Spacers received FDA 510(k) clearance under submission number K170157, sponsored by Globus Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-09-25.

Classification & Regulation

This clearance is catalogued under FDA product code OVD and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.