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FDA 510(k)

ORIGEN DBM WITH BIOACTIVE GLASS, NANOFUSE DBM

K-Number: K110976 · 2011-05-03

ApplicantNanotherapeutics, Inc.
Decision Date2011-05-03
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ORIGEN DBM WITH BIOACTIVE GLASS, NANOFUSE DBM is the device name listed in this FDA 510(k) record. The listed applicant is Nanotherapeutics, Inc.. It received FDA 510(k) clearance on 2011-05-03 under 510(k) number K110976. 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 ORIGEN DBM WITH BIOACTIVE GLASS, NANOFUSE DBM?

ORIGEN DBM WITH BIOACTIVE GLASS, NANOFUSE DBM is a medical device that received FDA 510(k) clearance on 2011-05-03. The listed applicant is Nanotherapeutics, Inc.. The 510(k) number is K110976.

When did ORIGEN DBM WITH BIOACTIVE GLASS, NANOFUSE DBM receive FDA 510(k) clearance?

ORIGEN DBM WITH BIOACTIVE GLASS, NANOFUSE DBM received FDA 510(k) clearance on 2011-05-03, under 510(k) number K110976.

Who is the listed applicant for ORIGEN DBM WITH BIOACTIVE GLASS, NANOFUSE DBM?

The FDA 510(k) record lists Nanotherapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORIGEN DBM WITH BIOACTIVE GLASS, NANOFUSE DBM?

The FDA product code for ORIGEN DBM WITH BIOACTIVE GLASS, NANOFUSE DBM is MQV.

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Official Source

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