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FDA 510(k)

FREEMAN/SAMUELSON TOTAL KNEE

K-Number: K830408 · 1983-02-24

ApplicantDepuy, Inc.
Decision Date1983-02-24
Product CodeMBV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FREEMAN/SAMUELSON TOTAL KNEE is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1983-02-24 under 510(k) number K830408. The device is classified under product code MBV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREEMAN/SAMUELSON TOTAL KNEE?

FREEMAN/SAMUELSON TOTAL KNEE is a medical device that received FDA 510(k) clearance on 1983-02-24. The listed applicant is Depuy, Inc.. The 510(k) number is K830408.

When did FREEMAN/SAMUELSON TOTAL KNEE receive FDA 510(k) clearance?

FREEMAN/SAMUELSON TOTAL KNEE received FDA 510(k) clearance on 1983-02-24, under 510(k) number K830408.

Who is the listed applicant for FREEMAN/SAMUELSON TOTAL 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 FREEMAN/SAMUELSON TOTAL KNEE?

The FDA product code for FREEMAN/SAMUELSON TOTAL KNEE is MBV.

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.

View all 303 devices →

Related Devices (Code: MBV)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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