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FDA 510(k)

LIVERPOOL KNEE PROSTHESIS

K-Number: K792325 · 1980-01-21

ApplicantDowns Surgical , Ltd.
Decision Date1980-01-21
Product CodeHRY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LIVERPOOL KNEE PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1980-01-21 under 510(k) number K792325. The device is classified under product code HRY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIVERPOOL KNEE PROSTHESIS?

LIVERPOOL KNEE PROSTHESIS is a medical device that received FDA 510(k) clearance on 1980-01-21. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K792325.

When did LIVERPOOL KNEE PROSTHESIS receive FDA 510(k) clearance?

LIVERPOOL KNEE PROSTHESIS received FDA 510(k) clearance on 1980-01-21, under 510(k) number K792325.

Who is the listed applicant for LIVERPOOL KNEE PROSTHESIS?

The FDA 510(k) record lists Downs Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIVERPOOL KNEE PROSTHESIS?

The FDA product code for LIVERPOOL KNEE PROSTHESIS is HRY.

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Related Devices (Code: HRY)

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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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