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FDA 510(k)

INTEGRA MOZAIK AND OS MOLDABLE MORSELS

K-Number: K091302 · 2009-12-04

ApplicantIntegra LifeSciences Corporation
Decision Date2009-12-04
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTEGRA MOZAIK AND OS MOLDABLE MORSELS is the device name listed in this FDA 510(k) record. The listed applicant is Integra LifeSciences Corporation. It received FDA 510(k) clearance on 2009-12-04 under 510(k) number K091302. 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 INTEGRA MOZAIK AND OS MOLDABLE MORSELS?

INTEGRA MOZAIK AND OS MOLDABLE MORSELS is a medical device that received FDA 510(k) clearance on 2009-12-04. The listed applicant is Integra LifeSciences Corporation. The 510(k) number is K091302.

When did INTEGRA MOZAIK AND OS MOLDABLE MORSELS receive FDA 510(k) clearance?

INTEGRA MOZAIK AND OS MOLDABLE MORSELS received FDA 510(k) clearance on 2009-12-04, under 510(k) number K091302.

Who is the listed applicant for INTEGRA MOZAIK AND OS MOLDABLE MORSELS?

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

What is the FDA product code for INTEGRA MOZAIK AND OS MOLDABLE MORSELS?

The FDA product code for INTEGRA MOZAIK AND OS MOLDABLE MORSELS 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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