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FDA 510(k)

DePuy Corail AMT Hip Prosthesis

K-Number: K173960 · 2018-09-21

ApplicantDepuy France S.A.S.
Decision Date2018-09-21
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DePuy Corail AMT Hip Prosthesis is a medical device manufactured by Depuy France S.A.S.. It received FDA 510(k) clearance on 2018-09-21 under approval number K173960. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DePuy Corail AMT Hip Prosthesis?

DePuy Corail AMT Hip Prosthesis is a medical device that received FDA 510(k) clearance on 2018-09-21. It is manufactured by Depuy France S.A.S.. The 510(k) number is K173960.

When was DePuy Corail AMT Hip Prosthesis approved by the FDA?

DePuy Corail AMT Hip Prosthesis received FDA 510(k) clearance on 2018-09-21, under approval number K173960.

What company makes DePuy Corail AMT Hip Prosthesis?

DePuy Corail AMT Hip Prosthesis is manufactured by Depuy France S.A.S..

What is the FDA product code for DePuy Corail AMT Hip Prosthesis?

The FDA product code for DePuy Corail AMT Hip Prosthesis is LZO.

Related Devices (Code: LZO)

K160895Initia Total Hip System & BIOCERAM AZUL(R) HEADKyocera Medical Corporation K161830Zimmer M/L Taper Hip ProsthesisZimmer, Inc. K161192Wagner SL Revision Stem Lateral, Wagner Cone Prosthesis® SystemZimmer GmbH K152893Corin Optimized Positioning System (OPS)Corin USA K160289MasterLoc StemMedacta International K152903REVIVAL(TM) Modular Revision Hip StemCorin USA

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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