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FDA 510(k)

Avenir Complete Hip System

K-Number: K182048 · 2018-12-07

ApplicantZimmer, Inc.
Decision Date2018-12-07
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Avenir Complete Hip System is a medical device manufactured by Zimmer, Inc.. It received FDA 510(k) clearance on 2018-12-07 under approval number K182048. 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 Avenir Complete Hip System?

Avenir Complete Hip System is a medical device that received FDA 510(k) clearance on 2018-12-07. It is manufactured by Zimmer, Inc.. The 510(k) number is K182048.

When was Avenir Complete Hip System approved by the FDA?

Avenir Complete Hip System received FDA 510(k) clearance on 2018-12-07, under approval number K182048.

What company makes Avenir Complete Hip System?

Avenir Complete Hip System is manufactured by Zimmer, Inc..

What is the FDA product code for Avenir Complete Hip System?

The FDA product code for Avenir Complete Hip System is LZO.

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Other Devices by Zimmer, Inc.

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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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