Avenir® Müller Stem; Avenir Complete™ Hip System
K-Number: K260182 · 2026-04-27
Device Summary
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. The listed applicant is Zimmer, Inc.. The 510(k) number is K260182.
When did Avenir® Müller Stem; Avenir Complete™ Hip System receive FDA 510(k) clearance?
Avenir® Müller Stem; Avenir Complete™ Hip System received FDA 510(k) clearance on 2026-04-27, under 510(k) number K260182.
Who is the listed applicant for Avenir® Müller Stem; Avenir Complete™ Hip System?
The FDA 510(k) record lists Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Zimmer, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LZO)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.