FDA 510(k)

Corin TaperFit Hip Stem

K-Number: K153725 · 2016-03-25

Decision Date2016-03-25

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Corin TaperFit Hip Stem is a medical device manufactured by Corin U.S.A. Limited. It received FDA 510(k) clearance on 2016-03-25 under approval number K153725. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Corin TaperFit Hip Stem?

Corin TaperFit Hip Stem is a medical device that received FDA 510(k) clearance on 2016-03-25. It is manufactured by Corin U.S.A. Limited. The 510(k) number is K153725.

When was Corin TaperFit Hip Stem approved by the FDA?

Corin TaperFit Hip Stem received FDA 510(k) clearance on 2016-03-25, under approval number K153725.

What company makes Corin TaperFit Hip Stem?

Corin TaperFit Hip Stem is manufactured by Corin U.S.A. Limited.

What is the FDA product code for Corin TaperFit Hip Stem?

The FDA product code for Corin TaperFit Hip Stem is JDI.

Other Devices by Corin U.S.A. Limited

K153772Corin TriFit TS Hip K153381Corin Metafix Hip Stem K170359Trinity Dual Mobility System K170808Unity Total Knee System K162942Corin MetaFix Hip Stem K172551Trinity PLUS Acetabular Shell

View all 21 devices →

Related Devices (Code: JDI)

K160923REDAPT Anteverted Cemented LinerSmith & Nephew, Inc. K153057FitRite Total Hip Arthroplasty SystemExcera Orthopedics, Inc. K153216Alpine Cemented Hip SystemOrtho Development Corporation K162125MALUC Total Hip Arthroplasty SystemSurgtech, Inc. K180973Libertas Hip Replacement SystemMaxx Orthopedics, Inc. K191414EXETER Centralizer, EXETER 2.5mm PlugStryker Orthopaedics

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.