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FDA 510(k)

NOVABONE MACROPOR-SI+ - BIOACTIVE BONE GRAFT

K-Number: K110925 · 2011-07-05

ApplicantNovabone Products, LLC
Decision Date2011-07-05
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NOVABONE MACROPOR-SI+ - BIOACTIVE BONE GRAFT is the device name listed in this FDA 510(k) record. The listed applicant is Novabone Products, LLC. It received FDA 510(k) clearance on 2011-07-05 under 510(k) number K110925. 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 NOVABONE MACROPOR-SI+ - BIOACTIVE BONE GRAFT?

NOVABONE MACROPOR-SI+ - BIOACTIVE BONE GRAFT is a medical device that received FDA 510(k) clearance on 2011-07-05. The listed applicant is Novabone Products, LLC. The 510(k) number is K110925.

When did NOVABONE MACROPOR-SI+ - BIOACTIVE BONE GRAFT receive FDA 510(k) clearance?

NOVABONE MACROPOR-SI+ - BIOACTIVE BONE GRAFT received FDA 510(k) clearance on 2011-07-05, under 510(k) number K110925.

Who is the listed applicant for NOVABONE MACROPOR-SI+ - BIOACTIVE BONE GRAFT?

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

What is the FDA product code for NOVABONE MACROPOR-SI+ - BIOACTIVE BONE GRAFT?

The FDA product code for NOVABONE MACROPOR-SI+ - BIOACTIVE BONE GRAFT is MQV.

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Related Devices (Code: 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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