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FDA 510(k)

OSSIPRO BONE SUBSTITUTE MATERIAL

K-Number: K062630 · 2007-06-28

ApplicantEtex Corp.
Decision Date2007-06-28
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSSIPRO BONE SUBSTITUTE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Etex Corp.. It received FDA 510(k) clearance on 2007-06-28 under 510(k) number K062630. 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 OSSIPRO BONE SUBSTITUTE MATERIAL?

OSSIPRO BONE SUBSTITUTE MATERIAL is a medical device that received FDA 510(k) clearance on 2007-06-28. The listed applicant is Etex Corp.. The 510(k) number is K062630.

When did OSSIPRO BONE SUBSTITUTE MATERIAL receive FDA 510(k) clearance?

OSSIPRO BONE SUBSTITUTE MATERIAL received FDA 510(k) clearance on 2007-06-28, under 510(k) number K062630.

Who is the listed applicant for OSSIPRO BONE SUBSTITUTE MATERIAL?

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

What is the FDA product code for OSSIPRO BONE SUBSTITUTE MATERIAL?

The FDA product code for OSSIPRO BONE SUBSTITUTE MATERIAL is MQV.

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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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