FDA 510(k)

TRIGEN STRAIGHT HUMERAL NAIL SYSTEM

K-Number: K032722 · 2003-10-01

Decision Date2003-10-01

Product CodeHSB

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TRIGEN STRAIGHT HUMERAL NAIL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2003-10-01 under 510(k) number K032722. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIGEN STRAIGHT HUMERAL NAIL SYSTEM?

TRIGEN STRAIGHT HUMERAL NAIL SYSTEM is a medical device that received FDA 510(k) clearance on 2003-10-01. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K032722.

When did TRIGEN STRAIGHT HUMERAL NAIL SYSTEM receive FDA 510(k) clearance?

TRIGEN STRAIGHT HUMERAL NAIL SYSTEM received FDA 510(k) clearance on 2003-10-01, under 510(k) number K032722.

Who is the listed applicant for TRIGEN STRAIGHT HUMERAL NAIL SYSTEM?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRIGEN STRAIGHT HUMERAL NAIL SYSTEM?

The FDA product code for TRIGEN STRAIGHT HUMERAL NAIL SYSTEM is HSB.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.