MedTrace Logo

Facial iD Customized Mandible Reconstruction Plates

NCT07245758 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2026-04-22

No results posted yet for this study

Summary

A retrospective post market follow up to confirm the safety and performance of Stryker's Customized Plates for Mandibular Reconstruction. The study is performed to confirm the product's performance and safety by systematically collecting clinical data on its use.

Conditions

  • Mandibular Fractures
  • Mandible Fracture
  • Mandible; Deformity
  • MANDIBLE
  • Orthognathic Surgical Procedures

Interventions

DEVICE

Mandibular reconstruction

Primary or secondary reconstruction of the mandible using customized Mandible Reconstruction Plate (referred to as CMRP)

Sponsors & Collaborators

  • Stryker Craniomaxillofacial

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-12-01
Primary Completion
2026-04-04
Completion
2026-04-04
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT07245758 on ClinicalTrials.gov