U.S., Oct. 29 -- ClinicalTrials.gov registry received information related to the study (NCT07221916) titled 'Stryker's Surgeon iD Mandible Reconstruction Plates: A Retrospective Post Market Follow Up' on July 31.
Brief 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.
Study Start Date: Dec. 01, 2024
Study Type: OBSERVATIONAL
Condition:
Mandible Fracture
Mandibular Reconstruction
Intervention:
DEVICE: Mandibular Reconstruction
Mandibular Reconstruction or mandibular fracture fixation using a Surgeon iD Mandible Reconstruction ...