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FDA 510(k)

LOCON VLS DISTAL RADIUS PLATE SYSTEM

K-Number: K042358 · 2004-10-07

ApplicantWrightmedicaltechnologyinc
Decision Date2004-10-07
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LOCON VLS DISTAL RADIUS PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2004-10-07 under 510(k) number K042358. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOCON VLS DISTAL RADIUS PLATE SYSTEM?

LOCON VLS DISTAL RADIUS PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2004-10-07. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K042358.

When did LOCON VLS DISTAL RADIUS PLATE SYSTEM receive FDA 510(k) clearance?

LOCON VLS DISTAL RADIUS PLATE SYSTEM received FDA 510(k) clearance on 2004-10-07, under 510(k) number K042358.

Who is the listed applicant for LOCON VLS DISTAL RADIUS PLATE SYSTEM?

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 LOCON VLS DISTAL RADIUS PLATE SYSTEM?

The FDA product code for LOCON VLS DISTAL RADIUS PLATE SYSTEM is KTT.

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Related Devices (Code: KTT)

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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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