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FDA 510(k)

HOWMEDICA HUMERAL INTERCALARY SYSTEM

K-Number: K984202 · 1999-02-05

ApplicantHowmedica, Inc.
Decision Date1999-02-05
Product CodeHSD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HOWMEDICA HUMERAL INTERCALARY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica, Inc.. It received FDA 510(k) clearance on 1999-02-05 under 510(k) number K984202. The device is classified under product code HSD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOWMEDICA HUMERAL INTERCALARY SYSTEM?

HOWMEDICA HUMERAL INTERCALARY SYSTEM is a medical device that received FDA 510(k) clearance on 1999-02-05. The listed applicant is Howmedica, Inc.. The 510(k) number is K984202.

When did HOWMEDICA HUMERAL INTERCALARY SYSTEM receive FDA 510(k) clearance?

HOWMEDICA HUMERAL INTERCALARY SYSTEM received FDA 510(k) clearance on 1999-02-05, under 510(k) number K984202.

Who is the listed applicant for HOWMEDICA HUMERAL INTERCALARY SYSTEM?

The FDA 510(k) record lists Howmedica, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOWMEDICA HUMERAL INTERCALARY SYSTEM?

The FDA product code for HOWMEDICA HUMERAL INTERCALARY SYSTEM is HSD.

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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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