Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)— 510(k) K253171

Name: FDA 510(k) clearance K253171
Creator: U.S. Food and Drug Administration
Published: 2026-01-15

Substantially Equivalent

Maxx Orthopedics, Inc.

FDA 510(k) clearance K253171 for Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem), Substantially Equivalent on 2026-01-15. Applicant: Maxx Orthopedics, Inc.. Device class: 2.

Clearance details

Applicant: Maxx Orthopedics, Inc.
Product code: Code LZO
Device class: Class 2
Regulation: 21 CFR 888.3353
Advisory panel: Orthopedic
Date received: 2025-09-26
Decision date: 2026-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norristown, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LZO

view all

K253948 — Momentum Acetabular Cup System2026-09-02
K261009 — MobileLink Acetabular Cup System 40mm ID Inserts (various)2026-07-06
K260831 — Z1 Hip System2026-06-16
K260182 — Avenir® Müller Stem; Avenir Complete Hip System2026-04-27
K260037 — implantcast Packaging System Update2026-03-30

More clearances from Maxx Orthopedics, Inc.

view all

K261563 — Freedom Total Knee System (E-Poly Tibial Liners)2026-08-07
K261609 — Freedom Partial Knee System2026-08-04
K252777 — Freedom Metaphyseal Cone Implants (Metaphyseal Cones)2025-10-31
K253314 — Freedom Infinia Total Knee System2025-10-29
K253144 — Freedom® Total Knee System Titan PCK Components2025-10-22

Adverse events under product code LZO

product code LZO

Death: 17
Injury: 12,942
Malfunction: 1,756
Total: 14,715

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.