Knee System - India CDSCO Medical Device Registration
Knee System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000076_0fd2ba5dabd0832843ccf85d9aeffc94_66ebf78e1dce8548351e8ce682fb45c4. This device is marketed under the brand name JOURNEY. The license holder is Smith & Nephew Healthcare Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO.
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Brand Name
JOURNEY
License Holder
Smith & Nephew Healthcare Pvt. Ltd.Device Class
Approving Authority
CDSCO
Product Information
"* Rheumatoid arthritis * Postโtraumatic arthritis, osteoarthritis, or degenerative arthritis * Failed osteotomies, unicompartmental replacement, or total knee replacement. * Posterior stabilized knee systems are designed for use in patients in primary and revision surgery, where the anterior and posterior cruciate ligaments are incompetent and the collateral ligaments remain intact. * Constrained knee systems are designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (JOURNEY) are incompetent. * Hinge knee systems are designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (JOURNEY) are absent or incompetent."
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