Stryker Facial iD Universal Plate Configurator: A Retrospective Post Market Follow Up to Confirm Safety and Performance
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device
Study Type: Observational
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.
Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:
• Patients who received a Stryker UPC plate for osteotomy, stabilization and rigid fixation of maxillofacial fractures or reconstruction as per routine clinical practice
• Patients for whom data on the primary outcome variable is available.
Locations
United States
New York
New York Center for Orthognathic and Maxillofacial Surgery
RECRUITING
New York
New York Center for Orthognathic and Maxillofacial Surgery, Lake Success, New York
RECRUITING
New York
Contact Information
Primary
Ilka Meinert, Ph.D.
ilka.meinert@stryker.com
+49 761 488 8290
Time Frame
Start Date: 2024-11-18
Estimated Completion Date: 2026-01-15
Participants
Target number of participants: 80
Related Therapeutic Areas
Sponsors
Leads: Stryker Craniomaxillofacial