meddevicedb.com FDA Device Reference

VICTORY™ Lumbar Plate System

K232318 Class II Traditional
Decision Date
2023-10-31
Sponsor / Applicant
Globus Medical, Inc.

Technical Specification

510(k) Submission ID K232318
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2023-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VICTORY™ Lumbar Plate System received FDA 510(k) clearance under submission number K232318, 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 2023-10-31.

Classification & Regulation

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