3M UPF PROXIMAL FEMUR REPLACEMENT SYSTEM
K-Number: K791823 · 1979-10-30
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Device Summary
Frequently Asked Questions
What is the 3M UPF PROXIMAL FEMUR REPLACEMENT SYSTEM?
3M UPF PROXIMAL FEMUR REPLACEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1979-10-30. The listed applicant is 3M Company. The 510(k) number is K791823.
When did 3M UPF PROXIMAL FEMUR REPLACEMENT SYSTEM receive FDA 510(k) clearance?
3M UPF PROXIMAL FEMUR REPLACEMENT SYSTEM received FDA 510(k) clearance on 1979-10-30, under 510(k) number K791823.
Who is the listed applicant for 3M UPF PROXIMAL FEMUR REPLACEMENT SYSTEM?
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 3M UPF PROXIMAL FEMUR REPLACEMENT SYSTEM?
The FDA product code for 3M UPF PROXIMAL FEMUR REPLACEMENT SYSTEM 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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