meddevicedb.com FDA Device Reference

Versalock Sterile Plating System

K262537 Class II Special
Decision Date
2026-08-19
Sponsor / Applicant
GM Dos Reis Industria e Comercio Ltda.

Technical Specification

510(k) Submission ID K262537
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2026-08-19
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Versalock Sterile Plating System received FDA 510(k) clearance under submission number K262537, sponsored by GM Dos Reis Industria e Comercio Ltda.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2026-08-19.

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.