ZIMMER BEADED THREADED ACETABULAR CUP
K-Number: K884658 · 1988-11-30
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Device Summary
Frequently Asked Questions
What is the ZIMMER BEADED THREADED ACETABULAR CUP?
ZIMMER BEADED THREADED ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 1988-11-30. The listed applicant is Zimmer, Inc.. The 510(k) number is K884658.
When did ZIMMER BEADED THREADED ACETABULAR CUP receive FDA 510(k) clearance?
ZIMMER BEADED THREADED ACETABULAR CUP received FDA 510(k) clearance on 1988-11-30, under 510(k) number K884658.
Who is the listed applicant for ZIMMER BEADED THREADED ACETABULAR CUP?
The FDA 510(k) record lists Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZIMMER BEADED THREADED ACETABULAR CUP?
The FDA product code for ZIMMER BEADED THREADED ACETABULAR CUP is KWY.
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 Zimmer, 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: KWY)
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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