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FDA 510(k)

T2 NAILING SYSTEM

K-Number: K032523 · 2003-10-22

ApplicantHowmedica Osteonics Corp.
Decision Date2003-10-22
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

T2 NAILING 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 2003-10-22 under 510(k) number K032523. 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 NAILING SYSTEM?

T2 NAILING SYSTEM is a medical device that received FDA 510(k) clearance on 2003-10-22. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K032523.

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

T2 NAILING SYSTEM received FDA 510(k) clearance on 2003-10-22, under 510(k) number K032523.

Who is the listed applicant for T2 NAILING 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 NAILING SYSTEM?

The FDA product code for T2 NAILING SYSTEM is HSB.

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Related Devices (Code: HSB)

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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