meddevicedb.com FDA Device Reference

Versalock Rib and Sternum Plates System

K232829 Class II Traditional
Decision Date
2024-06-26
Sponsor / Applicant
GM Dos Reis Industria e Comercio Ltda.

Technical Specification

510(k) Submission ID K232829
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2024-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Versalock Rib and Sternum Plates System received FDA 510(k) clearance under submission number K232829, sponsored by GM Dos Reis Industria e Comercio Ltda.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2024-06-26.

Classification & Regulation

This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.