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FDA 510(k)

ZYRANOX ZIRCONIA CERAMIC FEMORAL HEADS

K-Number: K992235 · 1999-11-23

ApplicantCorin USA
Decision Date1999-11-23
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZYRANOX ZIRCONIA CERAMIC FEMORAL HEADS is the device name listed in this FDA 510(k) record. The listed applicant is Corin USA. It received FDA 510(k) clearance on 1999-11-23 under 510(k) number K992235. 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 ZYRANOX ZIRCONIA CERAMIC FEMORAL HEADS?

ZYRANOX ZIRCONIA CERAMIC FEMORAL HEADS is a medical device that received FDA 510(k) clearance on 1999-11-23. The listed applicant is Corin USA. The 510(k) number is K992235.

When did ZYRANOX ZIRCONIA CERAMIC FEMORAL HEADS receive FDA 510(k) clearance?

ZYRANOX ZIRCONIA CERAMIC FEMORAL HEADS received FDA 510(k) clearance on 1999-11-23, under 510(k) number K992235.

Who is the listed applicant for ZYRANOX ZIRCONIA CERAMIC FEMORAL HEADS?

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

What is the FDA product code for ZYRANOX ZIRCONIA CERAMIC FEMORAL HEADS?

The FDA product code for ZYRANOX ZIRCONIA CERAMIC FEMORAL HEADS is LZO.

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Other records listing Corin USA as applicant

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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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