FDA 510(k)

Corin TriFit CF Hip Stem

K-Number: K173880 · 2018-04-11

Decision Date2018-04-11

Product CodeMEH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Corin TriFit CF Hip Stem is a medical device manufactured by Corin U.S.A. Limited. It received FDA 510(k) clearance on 2018-04-11 under approval 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. It is manufactured by Corin U.S.A. Limited. The 510(k) number is K173880.

When was Corin TriFit CF Hip Stem approved by the FDA?

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

What company makes Corin TriFit CF Hip Stem?

Corin TriFit CF Hip Stem is manufactured by Corin U.S.A. Limited.

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 Devices by Corin U.S.A. Limited

K153772Corin TriFit TS Hip K153725Corin TaperFit Hip Stem K153381Corin Metafix Hip Stem K170359Trinity Dual Mobility System K170808Unity Total Knee System K162942Corin MetaFix Hip Stem

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Related Devices (Code: MEH)

K153649Exactech® Novation® Element Press-fit Femoral StemExactech, Inc. K160011H-Max S stemLima Corporate S.P.A. K161155Origin Coxa Vara Hip StemSignature Orthopaedics Pty, Ltd. K160907DePuy Actis DuoFix Hip ProsthesisDepuy(Ireland) K153131Logical C-Series Acetabular Shell, Logical Constrained Liner, Logical Constrained Liner Collar, Logical 20° Hooded Acetabular LinerSignature Orthopaedics Pty, Ltd. K153772Corin TriFit TS HipCorin U.S.A. Limited

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.