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FDA 510(k)

WUJIN #3 TIBIAL NAIL

K-Number: K002325 · 2000-10-30

Decision Date2000-10-30
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WUJIN #3 TIBIAL NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Biologically Oriented Prostheses. It received FDA 510(k) clearance on 2000-10-30 under 510(k) number K002325. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WUJIN #3 TIBIAL NAIL?

WUJIN #3 TIBIAL NAIL is a medical device that received FDA 510(k) clearance on 2000-10-30. The listed applicant is Biologically Oriented Prostheses. The 510(k) number is K002325.

When did WUJIN #3 TIBIAL NAIL receive FDA 510(k) clearance?

WUJIN #3 TIBIAL NAIL received FDA 510(k) clearance on 2000-10-30, under 510(k) number K002325.

Who is the listed applicant for WUJIN #3 TIBIAL NAIL?

The FDA 510(k) record lists Biologically Oriented Prostheses as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WUJIN #3 TIBIAL NAIL?

The FDA product code for WUJIN #3 TIBIAL NAIL is JDS.

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 Biologically Oriented Prostheses 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 9 devices →

Related Devices (Code: JDS)

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

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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