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FDA 510(k)

BONESOURCE BVF

K-Number: K031435 · 2003-08-04

ApplicantHowmedica Osteonics
Decision Date2003-08-04
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BONESOURCE BVF is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics. It received FDA 510(k) clearance on 2003-08-04 under 510(k) number K031435. 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 BONESOURCE BVF?

BONESOURCE BVF is a medical device that received FDA 510(k) clearance on 2003-08-04. The listed applicant is Howmedica Osteonics. The 510(k) number is K031435.

When did BONESOURCE BVF receive FDA 510(k) clearance?

BONESOURCE BVF received FDA 510(k) clearance on 2003-08-04, under 510(k) number K031435.

Who is the listed applicant for BONESOURCE BVF?

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

What is the FDA product code for BONESOURCE BVF?

The FDA product code for BONESOURCE BVF is MQV.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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