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FDA 510(k)

OSSIMEND (TM) BONE GRAFT MATERIAL

K-Number: K052812 · 2006-01-25

ApplicantCollagen Matrix, Inc.
Decision Date2006-01-25
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSSIMEND (TM) BONE GRAFT MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Collagen Matrix, Inc.. It received FDA 510(k) clearance on 2006-01-25 under 510(k) number K052812. 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 OSSIMEND (TM) BONE GRAFT MATERIAL?

OSSIMEND (TM) BONE GRAFT MATERIAL is a medical device that received FDA 510(k) clearance on 2006-01-25. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K052812.

When did OSSIMEND (TM) BONE GRAFT MATERIAL receive FDA 510(k) clearance?

OSSIMEND (TM) BONE GRAFT MATERIAL received FDA 510(k) clearance on 2006-01-25, under 510(k) number K052812.

Who is the listed applicant for OSSIMEND (TM) BONE GRAFT MATERIAL?

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

What is the FDA product code for OSSIMEND (TM) BONE GRAFT MATERIAL?

The FDA product code for OSSIMEND (TM) BONE GRAFT MATERIAL is MQV.

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Other records listing Collagen Matrix, Inc. as applicant

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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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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