Knee System
- UID
- IMP/MD/2018/000445_0fd2ba5dabd0832843ccf85d9aeffc94_2f590968ac9a94e9f952aec452e4fceb
- Device class
- Class C
- Brand name
- Coonrad/ Morrey Total Elbow - Ulnar Component
- License holder
- M/s Zimmer India Pvt. Ltd
- Approving authority
- CDSCO
- Product information
- This device is indicated for patients with severe knee pain and disability due to: • Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis, • Collagen disorders, and/or avascular necrosis of the femoral condyle, • Post-traumatic loss of joint configuration, particularly when there is patellofemoral erosion, dysfunction or prior patellectomy. • Moderate valgus, varus, or flexion deformities. • The salvage of previously failed surgical attempts or for a knee in which satisfactory stability in flexion cannot be obtained at the time of surgery
Knee System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000445_0fd2ba5dabd0832843ccf85d9aeffc94_2f590968ac9a94e9f952aec452e4fceb. This device is marketed under the brand name Coonrad/ Morrey Total Elbow - Ulnar Component. The license holder is M/s Zimmer India Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is CDSCO.
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