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FDA 510(k)

WMT COMPOSITE DBM

K-Number: K083270 · 2009-08-27

ApplicantWrightmedicaltechnologyinc
Decision Date2009-08-27
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WMT COMPOSITE DBM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2009-08-27 under 510(k) number K083270. 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 WMT COMPOSITE DBM?

WMT COMPOSITE DBM is a medical device that received FDA 510(k) clearance on 2009-08-27. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K083270.

When did WMT COMPOSITE DBM receive FDA 510(k) clearance?

WMT COMPOSITE DBM received FDA 510(k) clearance on 2009-08-27, under 510(k) number K083270.

Who is the listed applicant for WMT COMPOSITE DBM?

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 WMT COMPOSITE DBM?

The FDA product code for WMT COMPOSITE DBM 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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