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FDA 510(k)

ALUMINA V40 FEMORAL HEADS

K-Number: K023901 · 2003-01-28

ApplicantHowmedica Osteonics Corp.
Decision Date2003-01-28
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALUMINA V40 FEMORAL HEADS 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 2003-01-28 under 510(k) number K023901. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALUMINA V40 FEMORAL HEADS?

ALUMINA V40 FEMORAL HEADS is a medical device that received FDA 510(k) clearance on 2003-01-28. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K023901.

When did ALUMINA V40 FEMORAL HEADS receive FDA 510(k) clearance?

ALUMINA V40 FEMORAL HEADS received FDA 510(k) clearance on 2003-01-28, under 510(k) number K023901.

Who is the listed applicant for ALUMINA V40 FEMORAL HEADS?

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 ALUMINA V40 FEMORAL HEADS?

The FDA product code for ALUMINA V40 FEMORAL HEADS is LZO.

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Related Devices (Code: LZO)

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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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