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FDA 510(k)

Gridlock Ankle Plating System

K-Number: K160177 · 2016-04-22

ApplicantTrilliant Surgical, Ltd.
Decision Date2016-04-22
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Gridlock Ankle Plating System is a medical device manufactured by Trilliant Surgical, Ltd.. It received FDA 510(k) clearance on 2016-04-22 under approval number K160177. 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 Gridlock Ankle Plating System?

Gridlock Ankle Plating System is a medical device that received FDA 510(k) clearance on 2016-04-22. It is manufactured by Trilliant Surgical, Ltd.. The 510(k) number is K160177.

When was Gridlock Ankle Plating System approved by the FDA?

Gridlock Ankle Plating System received FDA 510(k) clearance on 2016-04-22, under approval number K160177.

What company makes Gridlock Ankle Plating System?

Gridlock Ankle Plating System is manufactured by Trilliant Surgical, Ltd..

What is the FDA product code for Gridlock Ankle Plating System?

The FDA product code for Gridlock Ankle Plating System is HRS.

Related Clinical Trials

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Other Devices by Trilliant Surgical, Ltd.

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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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