Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00754637

Microplasty Tibial Tray Data Collection

Microplasty Tibial Tray Multi-Center Data Collection

Status
Withdrawn
Phase
Study type
Observational
Enrollment
0 (actual)
Sponsor
Zimmer Biomet · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this prospective clinical data-collection is to document the performance and clinical outcomes of the Microplasty Tibial Tray.

Detailed description

FDA has cleared this device via premarket notification 510(k) K063732. By being CE Marked, the Microplasty Tibial Tray also conforms to the essential requirements of EC Directive 93/42/EEC; in accordance to 13485:2003. The data gathered would be collated and used to provide feedback to design engineers, support marketing efforts, and answer potential questions from reimbursement agencies, and will serve as a part of Biomet's Post Market Surveillance System. Inclusion/exclusion criteria are identical to those indications and contraindications stated in the FDA approved labeling for the device in 510(k) K063732 Surgical techniques and patient care are to be standard for the surgeon participating in the protocol and should be maintained the same throughout the course of the data-collection. There will be no experimental or investigational devices used. There will be no experimental or investigational surgical techniques used. The devices and products will be used in accordance with their instructions for use and/or approved labeling. Any use of the device or collection of clinical data outside of the United States should comply with all local, state, and/or national and international regulations. Function will be assessed through the Knee Society Score . Survivorship will be documented by asking the surgeon to document revisions and complications.

Conditions

Timeline

Start date
2009-12-01
Primary completion
2022-12-01
Completion
2023-06-01
First posted
2008-09-18
Last updated
2017-06-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00754637. Inclusion in this directory is not an endorsement.