Spinal System
- UID
- IMP/MD/2019/000067_ef8f021e7311537e98cc9bb1be30fcab_2504dbfe00061cf6b3fbd3aa93873c29
- Device class
- Class C
- Brand name
- VLIFT
- License holder
- Stryker India Pvt. Ltd.,
- Approving authority
- CDSCO
- Product information
- The ES2TM Spinal System is intended for percutaneous, posterior, non-cervical pedicle and non-pedicle fixation of the spine to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion for the following indications: Degenerative disc disease (VLIFT) (VLIFT); Spondylolithesis; Trauma (VLIFT); Spinal Stenosis; Curvatures (VLIFT); Tumor; Pseudoarthrosis; and Failed pervious fusion. The Titanium and VitalliumR rods from the Stryker Spine RADIUSR, MANTISR and MANTISR Redux Spinal Systems are intended to be used with the other components of the ES2TM Spinal System
Spinal System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000067_ef8f021e7311537e98cc9bb1be30fcab_2504dbfe00061cf6b3fbd3aa93873c29. 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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