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FDA 510(k)

OSTEOSET DBM PELLETS, MODEL 8600-48XX

K-Number: K022828 · 2004-04-02

ApplicantWrightmedicaltechnologyinc
Decision Date2004-04-02
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEOSET DBM PELLETS, MODEL 8600-48XX is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2004-04-02 under 510(k) number K022828. 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 OSTEOSET DBM PELLETS, MODEL 8600-48XX?

OSTEOSET DBM PELLETS, MODEL 8600-48XX is a medical device that received FDA 510(k) clearance on 2004-04-02. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K022828.

When did OSTEOSET DBM PELLETS, MODEL 8600-48XX receive FDA 510(k) clearance?

OSTEOSET DBM PELLETS, MODEL 8600-48XX received FDA 510(k) clearance on 2004-04-02, under 510(k) number K022828.

Who is the listed applicant for OSTEOSET DBM PELLETS, MODEL 8600-48XX?

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 OSTEOSET DBM PELLETS, MODEL 8600-48XX?

The FDA product code for OSTEOSET DBM PELLETS, MODEL 8600-48XX 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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