meddevicedb.com FDA Device Reference

INDEPENDENCE SPACER

K120101 Class II Special
Decision Date
2012-03-27
Sponsor / Applicant
Globus Medical, Inc.

Technical Specification

510(k) Submission ID K120101
Product Code OVD
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2012-03-27
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INDEPENDENCE SPACER received FDA 510(k) clearance under submission number K120101, sponsored by Globus Medical, 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 2012-03-27.

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.