F-24 FEMORAL HIP PROSTHESIS
K-Number: K901687 · 1990-09-07
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Device Summary
Frequently Asked Questions
What is the F-24 FEMORAL HIP PROSTHESIS?
F-24 FEMORAL HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1990-09-07. The listed applicant is Med-Tek Corp.. The 510(k) number is K901687.
When did F-24 FEMORAL HIP PROSTHESIS receive FDA 510(k) clearance?
F-24 FEMORAL HIP PROSTHESIS received FDA 510(k) clearance on 1990-09-07, under 510(k) number K901687.
Who is the listed applicant for F-24 FEMORAL HIP PROSTHESIS?
The FDA 510(k) record lists Med-Tek Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for F-24 FEMORAL HIP PROSTHESIS?
The FDA product code for F-24 FEMORAL HIP PROSTHESIS 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 Med-Tek 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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