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FDA 510(k)

WROUGHT (FORGED) VITALLIUM

K-Number: K771408 · 1977-08-04

ApplicantHowmedica Corp.
Decision Date1977-08-04
Product CodeLZN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WROUGHT (FORGED) VITALLIUM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1977-08-04 under 510(k) number K771408. The device is classified under product code LZN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WROUGHT (FORGED) VITALLIUM?

WROUGHT (FORGED) VITALLIUM is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Howmedica Corp.. The 510(k) number is K771408.

When did WROUGHT (FORGED) VITALLIUM receive FDA 510(k) clearance?

WROUGHT (FORGED) VITALLIUM received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771408.

Who is the listed applicant for WROUGHT (FORGED) VITALLIUM?

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 WROUGHT (FORGED) VITALLIUM?

The FDA product code for WROUGHT (FORGED) VITALLIUM is LZN.

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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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