FDA 510(k)

HOWMEDICA T-III G ALLOY

K-Number: K810380 · 1981-03-17

Decision Date1981-03-17

Product CodeEJS

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

HOWMEDICA T-III G 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 1981-03-17 under 510(k) number K810380. 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 T-III G ALLOY?

HOWMEDICA T-III G ALLOY is a medical device that received FDA 510(k) clearance on 1981-03-17. The listed applicant is Howmedica Corp.. The 510(k) number is K810380.

When did HOWMEDICA T-III G ALLOY receive FDA 510(k) clearance?

HOWMEDICA T-III G ALLOY received FDA 510(k) clearance on 1981-03-17, under 510(k) number K810380.

Who is the listed applicant for HOWMEDICA T-III G 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 T-III G ALLOY?

The FDA product code for HOWMEDICA T-III G 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.