WebDownload scientific diagram The stabilization of the spine to the pelvis with Synthes SynMesh cylindrical cages. from publication: Total sacrectomy for recurrent rectal cancer – A case report ... Webarea or relatively close to the position of the SYNMESH device. Treatment before device is used Synthes products supplied in a non-sterile condition must be cleaned and steam-sterilized prior to surgical use. Prior to cleaning, remove all original packaging. Prior to …
Cervical interbody fusion cage - ACIS™ - Depuy Synthes - anterior
WebSYNMESH® CUTTER Synthes GmbH. FDA.report › GUDID › Synthes GmbH › 07611819744493. ... Synthes GmbH: Device Count: 1: DM Exempt: false: Pre-market Exempt: true: MRI Safety Status: Labeling does not contain MRI Safety Information: Human Cell/Tissue Product: false: Device Kit: false: Device Combination Product: WebApr 27, 2024 · Brand Name: SynMesh Version or Model: 495.357 Commercial Distribution Status: In Commercial Distribution Catalog Number: 495357 Company Name: Synthes GmbH Primary DI Number: 10705034785288 Issuing Agency: GS1 Commercial Distribution End Date: Device Count: 1 Labeler D-U-N-S® Number*: 486711679 * ... smsf land tax exemption
Surgical Techniquesynthes.vo.llnwd.net/o16/LLNWMB8/INT Mobile/Synthes …
http://synthes.vo.llnwd.net/o16/LLNWMB8/INT%20Mobile/Synthes%20International/Product%20Support%20Material/legacy_Synthes_PDF/DSEM-SPN-1215-0385-1_LR.pdf WebThe SynMesh system is indicated for use as a vertebral body replacement device in thoracolumbar spine (T1 through L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. This modular system allows building of the most appropriate construct to address the defect and patients anatomy. The SynMesh system is to be used … rkhbrd016aby1