CONTOUR FEMORAL HIP STEM WITH POROCOAT
K-Number: K926120 · 1993-03-31
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Device Summary
Frequently Asked Questions
What is the CONTOUR FEMORAL HIP STEM WITH POROCOAT?
CONTOUR FEMORAL HIP STEM WITH POROCOAT is a medical device that received FDA 510(k) clearance on 1993-03-31. The listed applicant is Depuy, Inc.. The 510(k) number is K926120.
When did CONTOUR FEMORAL HIP STEM WITH POROCOAT receive FDA 510(k) clearance?
CONTOUR FEMORAL HIP STEM WITH POROCOAT received FDA 510(k) clearance on 1993-03-31, under 510(k) number K926120.
Who is the listed applicant for CONTOUR FEMORAL HIP STEM WITH POROCOAT?
The FDA 510(k) record lists Depuy, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONTOUR FEMORAL HIP STEM WITH POROCOAT?
The FDA product code for CONTOUR FEMORAL HIP STEM WITH POROCOAT is KWL.
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 Depuy, 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: KWL)
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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