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FDA 510(k)

OSTEO IC RETROGRADE/ANTEGRADE FEMORAL NAIL NUT AND WASHER

K-Number: K990152 · 1999-03-15

ApplicantHowmedica Osteonics Corp.
Decision Date1999-03-15
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEO IC RETROGRADE/ANTEGRADE FEMORAL NAIL NUT AND WASHER 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 1999-03-15 under 510(k) number K990152. 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 OSTEO IC RETROGRADE/ANTEGRADE FEMORAL NAIL NUT AND WASHER?

OSTEO IC RETROGRADE/ANTEGRADE FEMORAL NAIL NUT AND WASHER is a medical device that received FDA 510(k) clearance on 1999-03-15. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K990152.

When did OSTEO IC RETROGRADE/ANTEGRADE FEMORAL NAIL NUT AND WASHER receive FDA 510(k) clearance?

OSTEO IC RETROGRADE/ANTEGRADE FEMORAL NAIL NUT AND WASHER received FDA 510(k) clearance on 1999-03-15, under 510(k) number K990152.

Who is the listed applicant for OSTEO IC RETROGRADE/ANTEGRADE FEMORAL NAIL NUT AND WASHER?

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 OSTEO IC RETROGRADE/ANTEGRADE FEMORAL NAIL NUT AND WASHER?

The FDA product code for OSTEO IC RETROGRADE/ANTEGRADE FEMORAL NAIL NUT AND WASHER 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.

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