FDA 510(k)

AMC R METACARPAL COMPONENT

K-Number: K790793 · 1979-06-22

Decision Date1979-06-22

Product CodeKWN

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

AMC R METACARPAL COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1979-06-22 under 510(k) number K790793. The device is classified under product code KWN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMC R METACARPAL COMPONENT?

AMC R METACARPAL COMPONENT is a medical device that received FDA 510(k) clearance on 1979-06-22. The listed applicant is Howmedica Corp.. The 510(k) number is K790793.

When did AMC R METACARPAL COMPONENT receive FDA 510(k) clearance?

AMC R METACARPAL COMPONENT received FDA 510(k) clearance on 1979-06-22, under 510(k) number K790793.

Who is the listed applicant for AMC R METACARPAL COMPONENT?

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 AMC R METACARPAL COMPONENT?

The FDA product code for AMC R METACARPAL COMPONENT is KWN.

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Other records listing Howmedica Corp. as applicant

K983528MICRO DYNAMIC MESH K983404TYPE 3 FEMORAL COMPONENTS K980926DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATION K980925DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATION K980626DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATION K980632DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION

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Related Devices (Code: KWN)

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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.