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RECRUITING
NCT07221916

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

Sponsor: Stryker Craniomaxillofacial

View on ClinicalTrials.gov

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.

Official title: Stryker Customized Plates for Mandibular Reconstruction: A Retrospective Post Market Follow Up to Confirm Safety and Performance of Surgeon iD Mandible Reconstruction Plates

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

50

Start Date

2024-12-01

Completion Date

2025-12-31

Last Updated

2025-10-28

Healthy Volunteers

No

Interventions

DEVICE

Mandibular Reconstruction

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

Locations (2)

UCSF Otolaryngology Head and Neck Surgery

San Francisco, California, United States

Heinrich-Braun-Klinikum gGmbH

Zwickau, Germany