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FDA 510(k)

Corin TriFit CF Hip Stem

K-Number: K173880 · 2018-04-11

ApplicantCorin U.S.A. Limited
Decision Date2018-04-11
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Corin TriFit CF Hip Stem is the device name listed in this FDA 510(k) record. The listed applicant is Corin U.S.A. Limited. It received FDA 510(k) clearance on 2018-04-11 under 510(k) number K173880. 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 Corin TriFit CF Hip Stem?

Corin TriFit CF Hip Stem is a medical device that received FDA 510(k) clearance on 2018-04-11. The listed applicant is Corin U.S.A. Limited. The 510(k) number is K173880.

When did Corin TriFit CF Hip Stem receive FDA 510(k) clearance?

Corin TriFit CF Hip Stem received FDA 510(k) clearance on 2018-04-11, under 510(k) number K173880.

Who is the listed applicant for Corin TriFit CF Hip Stem?

The FDA 510(k) record lists Corin U.S.A. Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Corin TriFit CF Hip Stem?

The FDA product code for Corin TriFit CF Hip Stem is MEH.

Other records listing Corin U.S.A. Limited as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242744Trinity EVO Acetabular ShellK241808ApolloHipX (THR.SS.0001)K241472Icona Hip StemK241570Unity Total Knee SystemK240875Unity Knee PS-C Tibial InsertK231172ApolloKnee

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Related Devices (Code: MEH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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