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FDA 510(k)

DUPONT DISTAL HUMERAL NAIL

K-Number: K890939 · 1989-05-22

ApplicantHowmedica Corp.
Decision Date1989-05-22
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DUPONT DISTAL HUMERAL NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1989-05-22 under 510(k) number K890939. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUPONT DISTAL HUMERAL NAIL?

DUPONT DISTAL HUMERAL NAIL is a medical device that received FDA 510(k) clearance on 1989-05-22. The listed applicant is Howmedica Corp.. The 510(k) number is K890939.

When did DUPONT DISTAL HUMERAL NAIL receive FDA 510(k) clearance?

DUPONT DISTAL HUMERAL NAIL received FDA 510(k) clearance on 1989-05-22, under 510(k) number K890939.

Who is the listed applicant for DUPONT DISTAL HUMERAL NAIL?

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 DUPONT DISTAL HUMERAL NAIL?

The FDA product code for DUPONT DISTAL HUMERAL NAIL is HRS.

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Other records listing Howmedica Corp. as applicant

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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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