meddevicedb.com FDA Device Reference

TRANSITION STABILIZATION SYSTEM

K073439 Class II Traditional
Decision Date
2009-02-20
Sponsor / Applicant
Globus Medical, Inc.

Technical Specification

510(k) Submission ID K073439
Product Code NQP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2009-02-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRANSITION STABILIZATION SYSTEM received FDA 510(k) clearance under submission number K073439, 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 2009-02-20.

Classification & Regulation

This clearance is catalogued under FDA product code NQP and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.