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FDA 510(k)

IGNITE BONE VOID FILLER KIT

K-Number: K052913 · 2005-11-07

ApplicantWrightmedicaltechnologyinc
Decision Date2005-11-07
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

IGNITE BONE VOID FILLER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2005-11-07 under 510(k) number K052913. 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 IGNITE BONE VOID FILLER KIT?

IGNITE BONE VOID FILLER KIT is a medical device that received FDA 510(k) clearance on 2005-11-07. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K052913.

When did IGNITE BONE VOID FILLER KIT receive FDA 510(k) clearance?

IGNITE BONE VOID FILLER KIT received FDA 510(k) clearance on 2005-11-07, under 510(k) number K052913.

Who is the listed applicant for IGNITE BONE VOID FILLER KIT?

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

What is the FDA product code for IGNITE BONE VOID FILLER KIT?

The FDA product code for IGNITE BONE VOID FILLER KIT is MQV.

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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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