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FDA 510(k)

INTEGRA MOZAIK BONE REGENERATION MATRIX - STRIPS

K-Number: K063124 · 2007-01-19

ApplicantIntegra Lifesciences Corp.
Decision Date2007-01-19
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTEGRA MOZAIK BONE REGENERATION MATRIX - STRIPS is the device name listed in this FDA 510(k) record. The listed applicant is Integra Lifesciences Corp.. It received FDA 510(k) clearance on 2007-01-19 under 510(k) number K063124. 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 BONE REGENERATION MATRIX - STRIPS?

INTEGRA MOZAIK BONE REGENERATION MATRIX - STRIPS is a medical device that received FDA 510(k) clearance on 2007-01-19. The listed applicant is Integra Lifesciences Corp.. The 510(k) number is K063124.

When did INTEGRA MOZAIK BONE REGENERATION MATRIX - STRIPS receive FDA 510(k) clearance?

INTEGRA MOZAIK BONE REGENERATION MATRIX - STRIPS received FDA 510(k) clearance on 2007-01-19, under 510(k) number K063124.

Who is the listed applicant for INTEGRA MOZAIK BONE REGENERATION MATRIX - STRIPS?

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

What is the FDA product code for INTEGRA MOZAIK BONE REGENERATION MATRIX - STRIPS?

The FDA product code for INTEGRA MOZAIK BONE REGENERATION MATRIX - STRIPS 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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