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FDA 510(k)

BONEMEDIK, AND BONEMEDIK-S

K-Number: K070897 · 2007-09-17

ApplicantMeta Biomed Co., Ltd.
Decision Date2007-09-17
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BONEMEDIK, AND BONEMEDIK-S is the device name listed in this FDA 510(k) record. The listed applicant is Meta Biomed Co., Ltd.. It received FDA 510(k) clearance on 2007-09-17 under 510(k) number K070897. 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 BONEMEDIK, AND BONEMEDIK-S?

BONEMEDIK, AND BONEMEDIK-S is a medical device that received FDA 510(k) clearance on 2007-09-17. The listed applicant is Meta Biomed Co., Ltd.. The 510(k) number is K070897.

When did BONEMEDIK, AND BONEMEDIK-S receive FDA 510(k) clearance?

BONEMEDIK, AND BONEMEDIK-S received FDA 510(k) clearance on 2007-09-17, under 510(k) number K070897.

Who is the listed applicant for BONEMEDIK, AND BONEMEDIK-S?

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

What is the FDA product code for BONEMEDIK, AND BONEMEDIK-S?

The FDA product code for BONEMEDIK, AND BONEMEDIK-S is 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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