Hip System
- UID
- IMP/MD/2018/000076_fe2aab42d294ab713b1f6619411cb39d_02bab1d60180d036a75150a8756844b5
- Device class
- Class D
- Brand name
- REFLECTION
- License holder
- Smith & Nephew Healthcare Pvt. Ltd.
- Approving authority
- CDSCO
- Product information
- Hip components are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or noninflammatory degenerative joint disease (REFLECTION) or any of its composite diagnoses of osteoarthritis, avascular necrosis, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant. Hip components are also indicated for inflammatory degenerative joint disease including rheumatoid arthritis, arthritis secondary to a variety of diseases and anomalies, and congenital dysplasia; treatments of nonunion, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement that are unmanageable using other techniques; endoprosthesis, femoral osteotomy, or Girdlestone resection; fracture-dislocation of the hip; and correction of deformity
Hip System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000076_fe2aab42d294ab713b1f6619411cb39d_02bab1d60180d036a75150a8756844b5. This device is marketed under the brand name REFLECTION. The license holder is Smith & Nephew Healthcare Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is CDSCO.
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