Stryker VLIFT® Vertebral Body Replacement System - HSA Registration DE0004760
Access comprehensive regulatory information for Stryker VLIFT® Vertebral Body Replacement System in the Singapore medical device market through Pure Global AI's free database. This CLASS C medical device is registered under HSA registration number DE0004760 and owned by Stryker Spine. The device was registered on February 13, 2010.
This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.
Intended to replace a vertebral body or an entire vertebra. It is for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body or vertebra resected or excised during total and partial corpectomy and vertebrectomy procedures due to tumor or trauma (i.e., fracture). For both, corpectomy and vertebrectomy procedures, VLIFT® system is intended to be used with supplemental internal fixation systems. The supplemental internal fixation systems that may be used with VLIFT® system include, but are not limited to, Stryker Spine plate or rod systems (Xia® Spinal System, Spiral Radius 90DTM and Trio®). The use of bone graft with the VLIFT® system is optional.