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FDA 510(k)

Avenir® Müller Stem; Avenir Complete™ Hip System

K-Number: K260182 · 2026-04-27

ApplicantZimmer, Inc.
Decision Date2026-04-27
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Avenir® Müller Stem; Avenir Complete™ Hip System is a medical device manufactured by Zimmer, Inc.. It received FDA 510(k) clearance on 2026-04-27 under approval number K260182. 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® Müller Stem; Avenir Complete™ Hip System?

Avenir® Müller Stem; Avenir Complete™ Hip System is a medical device that received FDA 510(k) clearance on 2026-04-27. It is manufactured by Zimmer, Inc.. The 510(k) number is K260182.

When was Avenir® Müller Stem; Avenir Complete™ Hip System approved by the FDA?

Avenir® Müller Stem; Avenir Complete™ Hip System received FDA 510(k) clearance on 2026-04-27, under approval number K260182.

What company makes Avenir® Müller Stem; Avenir Complete™ Hip System?

Avenir® Müller Stem; Avenir Complete™ Hip System is manufactured by Zimmer, Inc..

What is the FDA product code for Avenir® Müller Stem; Avenir Complete™ Hip System?

The FDA product code for Avenir® Müller Stem; Avenir Complete™ Hip System is LZO.

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Related Devices (Code: LZO)

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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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