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FDA 510(k)

ZIRCONIA CERAMIC MODULAR HEAD 9TYPE II TAPER

K-Number: K915641 · 1992-11-04

ApplicantBiomet, Inc.
Decision Date1992-11-04
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZIRCONIA CERAMIC MODULAR HEAD 9TYPE II TAPER is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1992-11-04 under 510(k) number K915641. 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 CERAMIC MODULAR HEAD 9TYPE II TAPER?

ZIRCONIA CERAMIC MODULAR HEAD 9TYPE II TAPER is a medical device that received FDA 510(k) clearance on 1992-11-04. The listed applicant is Biomet, Inc.. The 510(k) number is K915641.

When did ZIRCONIA CERAMIC MODULAR HEAD 9TYPE II TAPER receive FDA 510(k) clearance?

ZIRCONIA CERAMIC MODULAR HEAD 9TYPE II TAPER received FDA 510(k) clearance on 1992-11-04, under 510(k) number K915641.

Who is the listed applicant for ZIRCONIA CERAMIC MODULAR HEAD 9TYPE II TAPER?

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

What is the FDA product code for ZIRCONIA CERAMIC MODULAR HEAD 9TYPE II TAPER?

The FDA product code for ZIRCONIA CERAMIC MODULAR HEAD 9TYPE II TAPER is LZO.

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Other records listing Biomet, Inc. 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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