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FDA 510(k)

KINAMED ATH-HA & ATH-HA LONG TOTAL HIP

K-Number: K914843 · 1992-02-03

ApplicantKinamed, Inc.
Decision Date1992-02-03
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KINAMED ATH-HA & ATH-HA LONG TOTAL HIP is the device name listed in this FDA 510(k) record. The listed applicant is Kinamed, Inc.. It received FDA 510(k) clearance on 1992-02-03 under 510(k) number K914843. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINAMED ATH-HA & ATH-HA LONG TOTAL HIP?

KINAMED ATH-HA & ATH-HA LONG TOTAL HIP is a medical device that received FDA 510(k) clearance on 1992-02-03. The listed applicant is Kinamed, Inc.. The 510(k) number is K914843.

When did KINAMED ATH-HA & ATH-HA LONG TOTAL HIP receive FDA 510(k) clearance?

KINAMED ATH-HA & ATH-HA LONG TOTAL HIP received FDA 510(k) clearance on 1992-02-03, under 510(k) number K914843.

Who is the listed applicant for KINAMED ATH-HA & ATH-HA LONG TOTAL HIP?

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

What is the FDA product code for KINAMED ATH-HA & ATH-HA LONG TOTAL HIP?

The FDA product code for KINAMED ATH-HA & ATH-HA LONG TOTAL HIP is MEH.

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Other records listing Kinamed, Inc. as applicant

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Related Devices (Code: MEH)

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K261576Icona Hip StemCorin, Ltd.K250375Allure Hip Stem and Intramedullary PlugsWaldemar Link GmbH & Co. KGK251166Mfinity Femoral SystemMedacta International S.A.K251052Trivicta® Hip StemOrtho Development Corp.K242315Resolve Modular Revision Hip StemUnited Orthopedic CorporationK243839Alteon® HA Femoral StemsExactech, Inc.

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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