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FDA 510(k)

Corin TriFit TS Hip

K-Number: K153772 · 2016-03-31

ApplicantCorin U.S.A. Limited
Decision Date2016-03-31
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Corin TriFit TS Hip 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 2016-03-31 under 510(k) number K153772. 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 TS Hip?

Corin TriFit TS Hip is a medical device that received FDA 510(k) clearance on 2016-03-31. The listed applicant is Corin U.S.A. Limited. The 510(k) number is K153772.

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

Corin TriFit TS Hip received FDA 510(k) clearance on 2016-03-31, under 510(k) number K153772.

Who is the listed applicant for Corin TriFit TS Hip?

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 TS Hip?

The FDA product code for Corin TriFit TS Hip 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.

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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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