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FDA 510(k)

MICROWARE BONE PLATES AND BONE SCREWS

K-Number: K072562 · 2008-12-04

Decision Date2008-12-04
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MICROWARE BONE PLATES AND BONE SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Microware Precision Co., Ltd.. It received FDA 510(k) clearance on 2008-12-04 under 510(k) number K072562. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROWARE BONE PLATES AND BONE SCREWS?

MICROWARE BONE PLATES AND BONE SCREWS is a medical device that received FDA 510(k) clearance on 2008-12-04. The listed applicant is Microware Precision Co., Ltd.. The 510(k) number is K072562.

When did MICROWARE BONE PLATES AND BONE SCREWS receive FDA 510(k) clearance?

MICROWARE BONE PLATES AND BONE SCREWS received FDA 510(k) clearance on 2008-12-04, under 510(k) number K072562.

Who is the listed applicant for MICROWARE BONE PLATES AND BONE SCREWS?

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

What is the FDA product code for MICROWARE BONE PLATES AND BONE SCREWS?

The FDA product code for MICROWARE BONE PLATES AND BONE SCREWS is HRS.

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.

Other records listing Microware Precision 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.

View all 8 devices →

Related Devices (Code: HRS)

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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