COXA ACETABULAR CUP
K-Number: K871852 · 1988-02-18
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Device Summary
Frequently Asked Questions
What is the COXA ACETABULAR CUP?
COXA ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Thackray USA. The 510(k) number is K871852.
When did COXA ACETABULAR CUP receive FDA 510(k) clearance?
COXA ACETABULAR CUP received FDA 510(k) clearance on 1988-02-18, under 510(k) number K871852.
Who is the listed applicant for COXA ACETABULAR CUP?
The FDA 510(k) record lists Thackray USA as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COXA ACETABULAR CUP?
The FDA product code for COXA ACETABULAR CUP is JDI.
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 Thackray USA 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: JDI)
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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