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FDA 510(k)

INTER-HA HIP PROSTHESIS

K-Number: K921672 · 1992-08-07

ApplicantKirschner Medical Corp.
Decision Date1992-08-07
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTER-HA HIP PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1992-08-07 under 510(k) number K921672. 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 INTER-HA HIP PROSTHESIS?

INTER-HA HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1992-08-07. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K921672.

When did INTER-HA HIP PROSTHESIS receive FDA 510(k) clearance?

INTER-HA HIP PROSTHESIS received FDA 510(k) clearance on 1992-08-07, under 510(k) number K921672.

Who is the listed applicant for INTER-HA HIP PROSTHESIS?

The FDA 510(k) record lists Kirschner Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTER-HA HIP PROSTHESIS?

The FDA product code for INTER-HA HIP PROSTHESIS is MEH.

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Other records listing Kirschner Medical Corp. 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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