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FDA 510(k)

CALCIGEN-S BONE VOID FILER

K-Number: K013790 · 2002-06-11

ApplicantBiomet Orthopedics, Inc.
Decision Date2002-06-11
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CALCIGEN-S BONE VOID FILER is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Orthopedics, Inc.. It received FDA 510(k) clearance on 2002-06-11 under 510(k) number K013790. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALCIGEN-S BONE VOID FILER?

CALCIGEN-S BONE VOID FILER is a medical device that received FDA 510(k) clearance on 2002-06-11. The listed applicant is Biomet Orthopedics, Inc.. The 510(k) number is K013790.

When did CALCIGEN-S BONE VOID FILER receive FDA 510(k) clearance?

CALCIGEN-S BONE VOID FILER received FDA 510(k) clearance on 2002-06-11, under 510(k) number K013790.

Who is the listed applicant for CALCIGEN-S BONE VOID FILER?

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

What is the FDA product code for CALCIGEN-S BONE VOID FILER?

The FDA product code for CALCIGEN-S BONE VOID FILER is MQV.

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Related Devices (Code: MQV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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