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FDA 510(k)

HOWMEDICA AG-PD CROWN AND BRIDGE ALLOY

K-Number: K792008 · 1979-11-20

ApplicantHowmedica Corp.
Decision Date1979-11-20
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HOWMEDICA AG-PD CROWN AND BRIDGE ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1979-11-20 under 510(k) number K792008. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOWMEDICA AG-PD CROWN AND BRIDGE ALLOY?

HOWMEDICA AG-PD CROWN AND BRIDGE ALLOY is a medical device that received FDA 510(k) clearance on 1979-11-20. The listed applicant is Howmedica Corp.. The 510(k) number is K792008.

When did HOWMEDICA AG-PD CROWN AND BRIDGE ALLOY receive FDA 510(k) clearance?

HOWMEDICA AG-PD CROWN AND BRIDGE ALLOY received FDA 510(k) clearance on 1979-11-20, under 510(k) number K792008.

Who is the listed applicant for HOWMEDICA AG-PD CROWN AND BRIDGE ALLOY?

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 HOWMEDICA AG-PD CROWN AND BRIDGE ALLOY?

The FDA product code for HOWMEDICA AG-PD CROWN AND BRIDGE ALLOY is EJS.

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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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