WUJIN #3 TIBIAL NAIL
K-Number: K002325 · 2000-10-30
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Device Summary
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.
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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