Vertebral Body Replacement system - India CDSCO Medical Device Registration

Vertebral Body Replacement system is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000067_b2a6ee60c78309631d8cc97d51982169_5da15b415cbe40885d5ff03437d74e67. This device is marketed under the brand name VLIFT. The license holder is Stryker India Pvt. Ltd.,, and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered

Class Class C

Vertebral Body Replacement system

UID: IMP/MD/2019/000067_b2a6ee60c78309631d8cc97d51982169_5da15b415cbe40885d5ff03437d74e67

Brand Name

VLIFT

License Holder

Stryker India Pvt. Ltd.,

Device Class

Class C

Approving Authority

CDSCO

Product Information

The VLIFT system is a device intended to replace a vertebral body or an entire vertebra. It is for use in the thoracolumbar spine (VLIFT) 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 (VLIFT). 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 (VLIFT). The use of bone graft with the VLIFT system is optional