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SUSTAIN SPACER

K031302 Class II Traditional
Decision Date
2003-06-27
Sponsor / Applicant
Globus Medical, Inc.

Technical Specification

510(k) Submission ID K031302
Product Code MQP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2003-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUSTAIN SPACER received FDA 510(k) clearance under submission number K031302, 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 2003-06-27.

Classification & Regulation

This clearance is catalogued under FDA product code MQP and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.