WMT MODULAR ULNAR HEAD IMPLANT
K-Number: K020274 · 2002-02-22
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Device Summary
Frequently Asked Questions
What is the WMT MODULAR ULNAR HEAD IMPLANT?
WMT MODULAR ULNAR HEAD IMPLANT is a medical device that received FDA 510(k) clearance on 2002-02-22. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K020274.
When did WMT MODULAR ULNAR HEAD IMPLANT receive FDA 510(k) clearance?
WMT MODULAR ULNAR HEAD IMPLANT received FDA 510(k) clearance on 2002-02-22, under 510(k) number K020274.
Who is the listed applicant for WMT MODULAR ULNAR HEAD IMPLANT?
The FDA 510(k) record lists Wrightmedicaltechnologyinc as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WMT MODULAR ULNAR HEAD IMPLANT?
The FDA product code for WMT MODULAR ULNAR HEAD IMPLANT is KXE.
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 Wrightmedicaltechnologyinc 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: KXE)
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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