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FDA 510(k)

ALLOMATRIX CUSTOM

K-Number: K053319 · 2006-03-06

ApplicantWrightmedicaltechnologyinc
Decision Date2006-03-06
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALLOMATRIX CUSTOM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2006-03-06 under 510(k) number K053319. 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 ALLOMATRIX CUSTOM?

ALLOMATRIX CUSTOM is a medical device that received FDA 510(k) clearance on 2006-03-06. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K053319.

When did ALLOMATRIX CUSTOM receive FDA 510(k) clearance?

ALLOMATRIX CUSTOM received FDA 510(k) clearance on 2006-03-06, under 510(k) number K053319.

Who is the listed applicant for ALLOMATRIX CUSTOM?

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 ALLOMATRIX CUSTOM?

The FDA product code for ALLOMATRIX CUSTOM 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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