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Clinical Trial

MultiCenter IDE Study of the PEEK-OPTIMA™ Femoral Component vs a CoCr Alloy TKA Femoral Component of Similar Design

NCT: NCT06627673 · RECRUITING

NCT IDNCT06627673
StatusRECRUITING
Start Date2026-01-01
Completion2029-03-01
SponsorMaxx Orthopedics Inc (INDUSTRY)
First posted
Last updated

Brief Summary

The purpose of this investigational device exemption (IDE) study is to monitor the performance (safety and efficacy) of the Maxx Orthopedics, Freedom Total Knee® System, with a femoral component of similar design, manufactured from polyether-ether-ketone (PEEK).

Frequently Asked Questions

What is MultiCenter IDE Study of the PEEK-OPTIMA™ Femoral Component vs a CoCr Alloy TKA Femoral Component of Similar Design?

MultiCenter IDE Study of the PEEK-OPTIMA™ Femoral Component vs a CoCr Alloy TKA Femoral Component of Similar Design is a clinical trial registered under NCT06627673. Current status: RECRUITING.

What is the status of NCT06627673?

The current status of NCT06627673 (MultiCenter IDE Study of the PEEK-OPTIMA™ Femoral Component vs a CoCr Alloy TKA Femoral Component of Similar Design) is: RECRUITING.

When did MultiCenter IDE Study of the PEEK-OPTIMA™ Femoral Component vs a CoCr Alloy TKA Femoral Component of Similar Design start?

MultiCenter IDE Study of the PEEK-OPTIMA™ Femoral Component vs a CoCr Alloy TKA Femoral Component of Similar Design started on 2026-01-01.

Related Devices

K240863Freedom® Total Knee SystemMaxx Orthopedics, Inc. K241597Freedom® Total Knee System - Porous Tibial Base PlateMaxx Orthopedics, Inc. K250382Freedom Total Knee System (All-poly Tibial Plate)Maxx Orthopedics, Inc. K251717Freedom® Total Knee System – Titanium Tibial Base PlateMaxx Orthopedics, Inc. K253144Freedom® Total Knee System – Titan PCK ComponentsMaxx Orthopedics, Inc.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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