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FDA 510(k)

MOZAIK BONE REGENERATION MATRIX - PUTTY

K-Number: K062353 · 2006-12-20

ApplicantIntegra LifeSciences Corporation
Decision Date2006-12-20
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MOZAIK BONE REGENERATION MATRIX - PUTTY 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 2006-12-20 under 510(k) number K062353. 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 MOZAIK BONE REGENERATION MATRIX - PUTTY?

MOZAIK BONE REGENERATION MATRIX - PUTTY is a medical device that received FDA 510(k) clearance on 2006-12-20. The listed applicant is Integra LifeSciences Corporation. The 510(k) number is K062353.

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

MOZAIK BONE REGENERATION MATRIX - PUTTY received FDA 510(k) clearance on 2006-12-20, under 510(k) number K062353.

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

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 MOZAIK BONE REGENERATION MATRIX - PUTTY?

The FDA product code for MOZAIK BONE REGENERATION MATRIX - PUTTY 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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