meddevicedb.com FDA Device Reference

Versalock Upper Limb Plating System

K243740 Class II Traditional
Decision Date
2025-01-29
Sponsor / Applicant
GM Dos Reis Industria e Comercio Ltda.

Technical Specification

510(k) Submission ID K243740
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2025-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Versalock Upper Limb Plating System received FDA 510(k) clearance under submission number K243740, 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 2025-01-29.

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.