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FDA 510(k)

SRC TOTAL KNEE

K-Number: K841022 · 1984-06-25

Decision Date1984-06-25
Product Code
DecisionSubstantially Equivalent

Device Summary

SRC TOTAL KNEE is the device name listed in this FDA 510(k) record. The listed applicant is Joint Medical Products Corp.. It received FDA 510(k) clearance on 1984-06-25 under 510(k) number K841022. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SRC TOTAL KNEE?

SRC TOTAL KNEE is a medical device that received FDA 510(k) clearance on 1984-06-25. The listed applicant is Joint Medical Products Corp.. The 510(k) number is K841022.

When did SRC TOTAL KNEE receive FDA 510(k) clearance?

SRC TOTAL KNEE received FDA 510(k) clearance on 1984-06-25, under 510(k) number K841022.

Who is the listed applicant for SRC TOTAL KNEE?

The FDA 510(k) record lists Joint Medical Products Corp. as the applicant. This does not by itself establish the device manufacturer.

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 Joint Medical Products 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.

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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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