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FDA 510(k)

Super Upper Limbs Versalock Plating System

K-Number: K260390 · 2026-03-17

ApplicantGM Dos Reis Industria e Comercio Ltda.
Decision Date2026-03-17
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Super Upper Limbs Versalock Plating System is a medical device manufactured by GM Dos Reis Industria e Comercio Ltda.. It received FDA 510(k) clearance on 2026-03-17 under approval number K260390. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Super Upper Limbs Versalock Plating System?

Super Upper Limbs Versalock Plating System is a medical device that received FDA 510(k) clearance on 2026-03-17. It is manufactured by GM Dos Reis Industria e Comercio Ltda.. The 510(k) number is K260390.

When was Super Upper Limbs Versalock Plating System approved by the FDA?

Super Upper Limbs Versalock Plating System received FDA 510(k) clearance on 2026-03-17, under approval number K260390.

What company makes Super Upper Limbs Versalock Plating System?

Super Upper Limbs Versalock Plating System is manufactured by GM Dos Reis Industria e Comercio Ltda..

What is the FDA product code for Super Upper Limbs Versalock Plating System?

The FDA product code for Super Upper Limbs Versalock Plating System is HRS.

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Related Devices (Code: HRS)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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