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FDA 510(k)

ZIRCONIA ARTICUL/EZE FEMORAL BALLS

K-Number: K952088 · 1995-06-30

ApplicantDepuy, Inc.
Decision Date1995-06-30
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZIRCONIA ARTICUL/EZE FEMORAL BALLS is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1995-06-30 under 510(k) number K952088. 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 ZIRCONIA ARTICUL/EZE FEMORAL BALLS?

ZIRCONIA ARTICUL/EZE FEMORAL BALLS is a medical device that received FDA 510(k) clearance on 1995-06-30. The listed applicant is Depuy, Inc.. The 510(k) number is K952088.

When did ZIRCONIA ARTICUL/EZE FEMORAL BALLS receive FDA 510(k) clearance?

ZIRCONIA ARTICUL/EZE FEMORAL BALLS received FDA 510(k) clearance on 1995-06-30, under 510(k) number K952088.

Who is the listed applicant for ZIRCONIA ARTICUL/EZE FEMORAL BALLS?

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

What is the FDA product code for ZIRCONIA ARTICUL/EZE FEMORAL BALLS?

The FDA product code for ZIRCONIA ARTICUL/EZE FEMORAL BALLS 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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