POLYCENTRIC TOTAL KNEE METAL TIBIAL
K-Number: K792240 · 1979-12-05
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Device Summary
Frequently Asked Questions
What is the POLYCENTRIC TOTAL KNEE METAL TIBIAL?
POLYCENTRIC TOTAL KNEE METAL TIBIAL is a medical device that received FDA 510(k) clearance on 1979-12-05. The listed applicant is Howmedica Corp.. The 510(k) number is K792240.
When did POLYCENTRIC TOTAL KNEE METAL TIBIAL receive FDA 510(k) clearance?
POLYCENTRIC TOTAL KNEE METAL TIBIAL received FDA 510(k) clearance on 1979-12-05, under 510(k) number K792240.
Who is the listed applicant for POLYCENTRIC TOTAL KNEE METAL TIBIAL?
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 POLYCENTRIC TOTAL KNEE METAL TIBIAL?
The FDA product code for POLYCENTRIC TOTAL KNEE METAL TIBIAL is HSX.
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: HSX)
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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