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FDA 510(k)

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)

K-Number: K253171 · 2026-01-15

ApplicantMaxx Orthopedics, Inc.
Decision Date2026-01-15
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) is the device name listed in this FDA 510(k) record. The listed applicant is Maxx Orthopedics, Inc.. It received FDA 510(k) clearance on 2026-01-15 under 510(k) number K253171. 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 Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)?

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) is a medical device that received FDA 510(k) clearance on 2026-01-15. The listed applicant is Maxx Orthopedics, Inc.. The 510(k) number is K253171.

When did Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) receive FDA 510(k) clearance?

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) received FDA 510(k) clearance on 2026-01-15, under 510(k) number K253171.

Who is the listed applicant for Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)?

The FDA 510(k) record lists Maxx Orthopedics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)?

The FDA product code for Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) is LZO.

Related Clinical Trials

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.

NCT06627673MultiCenter IDE Study of the PEEK-OPTIMA™ Femoral Component vs a CoCr Alloy TKA Femoral Component of Similar DesignRECRUITINGNCT06627699Prospective, In-Vivo, Post-Market Safety and Efficacy Surveillance Registry of the MAXX Orthopedics, Freedom Total Knee® SystemRECRUITING

Other records listing Maxx Orthopedics, Inc. as applicant

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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.

K261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbHK252401implaFit® short stemsImplantcast GmbHK250450Coated hip implantsMedacta International S.A.

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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