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Stryker Facial iD Universal Plate Configurator: A Retrospective Post Market Follow Up

NCT07245810 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 726

Last updated 2026-04-22

No results posted yet for this study

Summary

A retrospective post market follow up to confirm safety and performance of Stryker's Facial iD Universal Plate Configurator (UPC) implants in the clinical setting. The study is performed to confirm the product's performance and safety by systematically collecting clinical data on its use.

Conditions

  • Mandibular Fractures
  • Facial Fracture
  • Maxilla Fracture
  • Orthognathic Surgical Procedures

Interventions

DEVICE

Orthognatic surgery, Reconstructive maxillofacial surgery, Mandible and maxillofacial trauma surgery

Osteotomy, Mandible and Maxillofacial reconstruction, Orthognathic surgery

Sponsors & Collaborators

  • Stryker Craniomaxillofacial

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-18
Primary Completion
2026-05-31
Completion
2026-05-31
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 NCT07245810 on ClinicalTrials.gov