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FDA 510(k)

GEOMEDIC ANAMETRIC TOTAL KNEE

K-Number: K760842 · 1976-10-20

ApplicantHowmedica Corp.
Decision Date1976-10-20
Product CodeHRY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GEOMEDIC ANAMETRIC TOTAL KNEE is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1976-10-20 under 510(k) number K760842. 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 GEOMEDIC ANAMETRIC TOTAL KNEE?

GEOMEDIC ANAMETRIC TOTAL KNEE is a medical device that received FDA 510(k) clearance on 1976-10-20. The listed applicant is Howmedica Corp.. The 510(k) number is K760842.

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

GEOMEDIC ANAMETRIC TOTAL KNEE received FDA 510(k) clearance on 1976-10-20, under 510(k) number K760842.

Who is the listed applicant for GEOMEDIC ANAMETRIC TOTAL KNEE?

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 GEOMEDIC ANAMETRIC TOTAL KNEE?

The FDA product code for GEOMEDIC ANAMETRIC TOTAL KNEE is 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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