GRIPPER II ACETABULAR CUP
K-Number: K893584 · 1989-07-28
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Device Summary
Frequently Asked Questions
What is the GRIPPER II ACETABULAR CUP?
GRIPPER II ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 1989-07-28. The listed applicant is Joint Medical Products Corp.. The 510(k) number is K893584.
When did GRIPPER II ACETABULAR CUP receive FDA 510(k) clearance?
GRIPPER II ACETABULAR CUP received FDA 510(k) clearance on 1989-07-28, under 510(k) number K893584.
Who is the listed applicant for GRIPPER II ACETABULAR CUP?
The FDA 510(k) record lists Joint Medical Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GRIPPER II ACETABULAR CUP?
The FDA product code for GRIPPER II ACETABULAR CUP is LWJ.
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 Joint Medical Products Corp. 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: LWJ)
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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