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FDA 510(k)

KENSEY NASH BONE VOID FILLER XC

K-Number: K120141 · 2012-05-04

ApplicantKensey Nash Cororation
Decision Date2012-05-04
Product CodeMQV
Advisory CommitteeOR
DecisionUnknown

Device Summary

KENSEY NASH BONE VOID FILLER XC is the device name listed in this FDA 510(k) record. The listed applicant is Kensey Nash Cororation. It received FDA 510(k) clearance on 2012-05-04 under 510(k) number K120141. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the KENSEY NASH BONE VOID FILLER XC?

KENSEY NASH BONE VOID FILLER XC is a medical device that received FDA 510(k) clearance on 2012-05-04. The listed applicant is Kensey Nash Cororation. The 510(k) number is K120141.

When did KENSEY NASH BONE VOID FILLER XC receive FDA 510(k) clearance?

KENSEY NASH BONE VOID FILLER XC received FDA 510(k) clearance on 2012-05-04, under 510(k) number K120141.

Who is the listed applicant for KENSEY NASH BONE VOID FILLER XC?

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

What is the FDA product code for KENSEY NASH BONE VOID FILLER XC?

The FDA product code for KENSEY NASH BONE VOID FILLER XC 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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