ACETABULAR SHELLS & LINERS FOR ATH TOTAL HIP SYST.
K-Number: K893821 · 1989-11-06
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Device Summary
Frequently Asked Questions
What is the ACETABULAR SHELLS & LINERS FOR ATH TOTAL HIP SYST.?
ACETABULAR SHELLS & LINERS FOR ATH TOTAL HIP SYST. is a medical device that received FDA 510(k) clearance on 1989-11-06. The listed applicant is Kinamed, Inc.. The 510(k) number is K893821.
When did ACETABULAR SHELLS & LINERS FOR ATH TOTAL HIP SYST. receive FDA 510(k) clearance?
ACETABULAR SHELLS & LINERS FOR ATH TOTAL HIP SYST. received FDA 510(k) clearance on 1989-11-06, under 510(k) number K893821.
Who is the listed applicant for ACETABULAR SHELLS & LINERS FOR ATH TOTAL HIP SYST.?
The FDA 510(k) record lists Kinamed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACETABULAR SHELLS & LINERS FOR ATH TOTAL HIP SYST.?
The FDA product code for ACETABULAR SHELLS & LINERS FOR ATH TOTAL HIP SYST. 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 Kinamed, Inc. 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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