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FDA 510(k)

GRIDLOCK PLATING SYSTEM

K-Number: K123525 · 2013-02-15

Decision Date2013-02-15
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GRIDLOCK PLATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Trilliant Surgical, Ltd.. It received FDA 510(k) clearance on 2013-02-15 under 510(k) number K123525. 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 PLATING SYSTEM?

GRIDLOCK PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2013-02-15. The listed applicant is Trilliant Surgical, Ltd.. The 510(k) number is K123525.

When did GRIDLOCK PLATING SYSTEM receive FDA 510(k) clearance?

GRIDLOCK PLATING SYSTEM received FDA 510(k) clearance on 2013-02-15, under 510(k) number K123525.

Who is the listed applicant for GRIDLOCK PLATING SYSTEM?

The FDA 510(k) record lists Trilliant Surgical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRIDLOCK PLATING SYSTEM?

The FDA product code for GRIDLOCK PLATING SYSTEM is HRS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Trilliant Surgical, Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 14 devices →

Related Devices (Code: HRS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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