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Stryker's Surgeon iD Mandible Reconstruction Plates: A Retrospective Post Market Follow Up

NCT07221916 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 70

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 Surgeon iD Plates (SMRP) medical device. The study is performed to confirm the product's performance and safety by systematically collecting clinical data on its use.

Conditions

  • Mandible Fracture
  • Mandibular Reconstruction

Interventions

DEVICE

Mandibular Reconstruction

Mandibular Reconstruction or mandibular fracture fixation using a Surgeon iD Mandible Reconstruction Plate (referred to as Surgeon iD Plates).

Sponsors & Collaborators

  • Stryker Craniomaxillofacial

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-12-01
Primary Completion
2026-02-27
Completion
2026-02-27

Countries

  • United States
  • Germany

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 NCT07221916 on ClinicalTrials.gov