PROSTHESIS, VIDAL TOTAL HIP
K-Number: K770472 · 1977-03-17
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Device Summary
Frequently Asked Questions
What is the PROSTHESIS, VIDAL TOTAL HIP?
PROSTHESIS, VIDAL TOTAL HIP is a medical device that received FDA 510(k) clearance on 1977-03-17. The listed applicant is Howmedica Corp.. The 510(k) number is K770472.
When did PROSTHESIS, VIDAL TOTAL HIP receive FDA 510(k) clearance?
PROSTHESIS, VIDAL TOTAL HIP received FDA 510(k) clearance on 1977-03-17, under 510(k) number K770472.
Who is the listed applicant for PROSTHESIS, VIDAL TOTAL HIP?
The FDA 510(k) record lists Howmedica Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROSTHESIS, VIDAL TOTAL HIP?
The FDA product code for PROSTHESIS, VIDAL TOTAL HIP is JDL.
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 Howmedica 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: JDL)
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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