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FDA 510(k)

S2 FEMORAL NAIL

K-Number: K022461 · 2002-08-22

ApplicantHowmedica Osteonics
Decision Date2002-08-22
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

S2 FEMORAL NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics. It received FDA 510(k) clearance on 2002-08-22 under 510(k) number K022461. 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 S2 FEMORAL NAIL?

S2 FEMORAL NAIL is a medical device that received FDA 510(k) clearance on 2002-08-22. The listed applicant is Howmedica Osteonics. The 510(k) number is K022461.

When did S2 FEMORAL NAIL receive FDA 510(k) clearance?

S2 FEMORAL NAIL received FDA 510(k) clearance on 2002-08-22, under 510(k) number K022461.

Who is the listed applicant for S2 FEMORAL NAIL?

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

What is the FDA product code for S2 FEMORAL NAIL?

The FDA product code for S2 FEMORAL NAIL is 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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