TOTAL TIBIAL KNEE
K-Number: K761278 · 1977-01-05
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Device Summary
Frequently Asked Questions
What is the TOTAL TIBIAL KNEE?
TOTAL TIBIAL KNEE is a medical device that received FDA 510(k) clearance on 1977-01-05. The listed applicant is Depuy, Inc.. The 510(k) number is K761278.
When did TOTAL TIBIAL KNEE receive FDA 510(k) clearance?
TOTAL TIBIAL KNEE received FDA 510(k) clearance on 1977-01-05, under 510(k) number K761278.
Who is the listed applicant for TOTAL TIBIAL KNEE?
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 TOTAL TIBIAL KNEE?
The FDA product code for TOTAL TIBIAL KNEE is HRY.
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: HRY)
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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