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FDA 510(k)

TRILLIANT SURGICAL K-WIRES

K-Number: K121008 · 2012-06-04

ApplicantTrilliant Surgical, Ltd.
Decision Date2012-06-04
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRILLIANT SURGICAL K-WIRES 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 2012-06-04 under 510(k) number K121008. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRILLIANT SURGICAL K-WIRES?

TRILLIANT SURGICAL K-WIRES is a medical device that received FDA 510(k) clearance on 2012-06-04. The listed applicant is Trilliant Surgical, Ltd.. The 510(k) number is K121008.

When did TRILLIANT SURGICAL K-WIRES receive FDA 510(k) clearance?

TRILLIANT SURGICAL K-WIRES received FDA 510(k) clearance on 2012-06-04, under 510(k) number K121008.

Who is the listed applicant for TRILLIANT SURGICAL K-WIRES?

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 TRILLIANT SURGICAL K-WIRES?

The FDA product code for TRILLIANT SURGICAL K-WIRES is HTY.

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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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