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Total Temporomandibular Joint Replacement System Post Approval Study

NCT00762944 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 93

Last updated 2024-06-21

No results posted yet for this study

Summary

Post-Approval Study (PMA CoA) in Order to Obtain Additional Long Term Safety and Effectiveness Data \[PMA P020016\]

Conditions

  • Arthroplasty

Interventions

DEVICE

Biomet TMJ Replacement System

Total replacement of the temporomandibular joint with a Biomet TMJ Replacement System

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Oscar A Gonzalez, MD, DNP · Zimmer Biomet

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-09-21
Primary Completion
2008-08-25
Completion
2008-09-21
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00762944 on ClinicalTrials.gov