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FDA 510(k)

APAPORE BONE GRAFT SUBSTITUTE

K-Number: K033722 · 2004-05-07

ApplicantApatech , Ltd.
Decision Date2004-05-07
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

APAPORE BONE GRAFT SUBSTITUTE is the device name listed in this FDA 510(k) record. The listed applicant is Apatech , Ltd.. It received FDA 510(k) clearance on 2004-05-07 under 510(k) number K033722. 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 APAPORE BONE GRAFT SUBSTITUTE?

APAPORE BONE GRAFT SUBSTITUTE is a medical device that received FDA 510(k) clearance on 2004-05-07. The listed applicant is Apatech , Ltd.. The 510(k) number is K033722.

When did APAPORE BONE GRAFT SUBSTITUTE receive FDA 510(k) clearance?

APAPORE BONE GRAFT SUBSTITUTE received FDA 510(k) clearance on 2004-05-07, under 510(k) number K033722.

Who is the listed applicant for APAPORE BONE GRAFT SUBSTITUTE?

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

What is the FDA product code for APAPORE BONE GRAFT SUBSTITUTE?

The FDA product code for APAPORE BONE GRAFT SUBSTITUTE is MQV.

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Other records listing Apatech , Ltd. as applicant

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Related Devices (Code: MQV)

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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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