VS22 HIP PROSTHESIS
K-Number: K896266 · 1989-11-22
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Device Summary
Frequently Asked Questions
What is the VS22 HIP PROSTHESIS?
VS22 HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1989-11-22. The listed applicant is 3M Company. The 510(k) number is K896266.
When did VS22 HIP PROSTHESIS receive FDA 510(k) clearance?
VS22 HIP PROSTHESIS received FDA 510(k) clearance on 1989-11-22, under 510(k) number K896266.
Who is the listed applicant for VS22 HIP PROSTHESIS?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VS22 HIP PROSTHESIS?
The FDA product code for VS22 HIP PROSTHESIS 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 3M Company 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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