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FDA 510(k)

OSTEO-LINK BONE VOID FILLER PELLETS

K-Number: K060809 · 2006-07-03

Decision Date2006-07-03
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEO-LINK BONE VOID FILLER PELLETS is the device name listed in this FDA 510(k) record. The listed applicant is Promed Advance Technology Co., Ltd.. It received FDA 510(k) clearance on 2006-07-03 under 510(k) number K060809. 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 OSTEO-LINK BONE VOID FILLER PELLETS?

OSTEO-LINK BONE VOID FILLER PELLETS is a medical device that received FDA 510(k) clearance on 2006-07-03. The listed applicant is Promed Advance Technology Co., Ltd.. The 510(k) number is K060809.

When did OSTEO-LINK BONE VOID FILLER PELLETS receive FDA 510(k) clearance?

OSTEO-LINK BONE VOID FILLER PELLETS received FDA 510(k) clearance on 2006-07-03, under 510(k) number K060809.

Who is the listed applicant for OSTEO-LINK BONE VOID FILLER PELLETS?

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

What is the FDA product code for OSTEO-LINK BONE VOID FILLER PELLETS?

The FDA product code for OSTEO-LINK BONE VOID FILLER PELLETS is MQV.

Related Clinical Trials

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.

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.

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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