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FDA 510(k)

TIE-IN TRAPEZIUM

K-Number: K033529 · 2003-12-03

ApplicantWrightmedicaltechnologyinc
Decision Date2003-12-03
Product CodeKYI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TIE-IN TRAPEZIUM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2003-12-03 under 510(k) number K033529. The device is classified under product code KYI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIE-IN TRAPEZIUM?

TIE-IN TRAPEZIUM is a medical device that received FDA 510(k) clearance on 2003-12-03. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K033529.

When did TIE-IN TRAPEZIUM receive FDA 510(k) clearance?

TIE-IN TRAPEZIUM received FDA 510(k) clearance on 2003-12-03, under 510(k) number K033529.

Who is the listed applicant for TIE-IN TRAPEZIUM?

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

What is the FDA product code for TIE-IN TRAPEZIUM?

The FDA product code for TIE-IN TRAPEZIUM is KYI.

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Related Devices (Code: KYI)

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.

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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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