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FDA 510(k)

T2 ARTHRODESIS NAIL SYSTEM

K-Number: K020384 · 2002-05-06

ApplicantHowmedica Osteonics Corp.
Decision Date2002-05-06
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

T2 ARTHRODESIS NAIL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 2002-05-06 under 510(k) number K020384. 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 T2 ARTHRODESIS NAIL SYSTEM?

T2 ARTHRODESIS NAIL SYSTEM is a medical device that received FDA 510(k) clearance on 2002-05-06. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K020384.

When did T2 ARTHRODESIS NAIL SYSTEM receive FDA 510(k) clearance?

T2 ARTHRODESIS NAIL SYSTEM received FDA 510(k) clearance on 2002-05-06, under 510(k) number K020384.

Who is the listed applicant for T2 ARTHRODESIS NAIL SYSTEM?

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

What is the FDA product code for T2 ARTHRODESIS NAIL SYSTEM?

The FDA product code for T2 ARTHRODESIS NAIL SYSTEM is HSB.

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Related Devices (Code: HSB)

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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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