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FDA 510(k)

COMPORUS

K-Number: K062691 · 2008-04-15

ApplicantTakiron Co., Ltd.
Decision Date2008-04-15
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COMPORUS is the device name listed in this FDA 510(k) record. The listed applicant is Takiron Co., Ltd.. It received FDA 510(k) clearance on 2008-04-15 under 510(k) number K062691. 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 COMPORUS?

COMPORUS is a medical device that received FDA 510(k) clearance on 2008-04-15. The listed applicant is Takiron Co., Ltd.. The 510(k) number is K062691.

When did COMPORUS receive FDA 510(k) clearance?

COMPORUS received FDA 510(k) clearance on 2008-04-15, under 510(k) number K062691.

Who is the listed applicant for COMPORUS?

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

What is the FDA product code for COMPORUS?

The FDA product code for COMPORUS is MQV.

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Other records listing Takiron Co., Ltd. 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.

K081390BIOACTIF OSTEOTRANS INTERFENCE SCREWK073006OSTEOTRANS -MX BIOABSORBABLE BONE FIXATION SYSTEMK073312OSTEOTRANS-OT SCREWK073311OSTEOTRANS-OT PINK061881OSTEOTRANS -MX BIOABSORBABLE BONE FIXATION SYSTEM

Related Devices (Code: MQV)

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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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