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FDA 510(k)

VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE

K-Number: K072184 · 2007-09-18

Decision Date2007-09-18
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE is the device name listed in this FDA 510(k) record. The listed applicant is Orthovita, Inc.. It received FDA 510(k) clearance on 2007-09-18 under 510(k) number K072184. 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 VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE?

VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE is a medical device that received FDA 510(k) clearance on 2007-09-18. The listed applicant is Orthovita, Inc.. The 510(k) number is K072184.

When did VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE receive FDA 510(k) clearance?

VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE received FDA 510(k) clearance on 2007-09-18, under 510(k) number K072184.

Who is the listed applicant for VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE?

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

What is the FDA product code for VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE?

The FDA product code for VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE is MQV.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Orthovita, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: MQV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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