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FDA 510(k)

HOWMEDICA ALUMINA FEMORAL HEAD

K-Number: K945091 · 1995-01-18

ApplicantHowmedica Corp.
Decision Date1995-01-18
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HOWMEDICA ALUMINA FEMORAL HEAD is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1995-01-18 under 510(k) number K945091. 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 HOWMEDICA ALUMINA FEMORAL HEAD?

HOWMEDICA ALUMINA FEMORAL HEAD is a medical device that received FDA 510(k) clearance on 1995-01-18. The listed applicant is Howmedica Corp.. The 510(k) number is K945091.

When did HOWMEDICA ALUMINA FEMORAL HEAD receive FDA 510(k) clearance?

HOWMEDICA ALUMINA FEMORAL HEAD received FDA 510(k) clearance on 1995-01-18, under 510(k) number K945091.

Who is the listed applicant for HOWMEDICA ALUMINA FEMORAL HEAD?

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

What is the FDA product code for HOWMEDICA ALUMINA FEMORAL HEAD?

The FDA product code for HOWMEDICA ALUMINA FEMORAL HEAD is LZO.

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Other records listing Howmedica Corp. as applicant

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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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