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FDA 510(k)

MIMIX MP BONE VOID FILLER

K-Number: K043280 · 2004-12-21

ApplicantBiomet, Inc.
Decision Date2004-12-21
Product CodeGXP
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MIMIX MP BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2004-12-21 under 510(k) number K043280. The device is classified under product code GXP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIMIX MP BONE VOID FILLER?

MIMIX MP BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2004-12-21. The listed applicant is Biomet, Inc.. The 510(k) number is K043280.

When did MIMIX MP BONE VOID FILLER receive FDA 510(k) clearance?

MIMIX MP BONE VOID FILLER received FDA 510(k) clearance on 2004-12-21, under 510(k) number K043280.

Who is the listed applicant for MIMIX MP BONE VOID FILLER?

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 MIMIX MP BONE VOID FILLER?

The FDA product code for MIMIX MP BONE VOID FILLER is GXP.

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Other records listing Biomet, Inc. as applicant

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Related Devices (Code: GXP)

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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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