CDSCO UID MFG/MD/2019/000214_34c2e41e8e18584bcde6363d92a64ef3_26bf76ff30bc0a576b551cc5fe2fd4b5

Total Knee Replacement System

TTK HEALTHCARE LIMITED (ORTHO DIVISION)·Device Class Class C·India CDSCO·Brand: Altius
Registration details
UID
MFG/MD/2019/000214_34c2e41e8e18584bcde6363d92a64ef3_26bf76ff30bc0a576b551cc5fe2fd4b5
Device class
Class C
Brand name
Altius
Approving authority
Central Drug Standard Control Organisation, South Zone
Product information
Model Name: a.Buechel-Pappas High Flex Total Knee Replacement System, b. Buechel-Pappas High Flex Total Knee Replacement System – Mark IV - Total Knee Replacement System is intended to provide primary or revision options to the surgeons to reduce or eliminate pain, restore motion, and/or correct deformity. Model Name : c. Buechel-Pappas Revision Knee Replacement System-i. Co-Cr Mobile Bearing Revision Knee – Cemented -This Buechel-Pappas (Altius) Revision Knee Replacement System is intended to provide primary or revision options to the surgeon to correct severe deformity and/or reduce or eliminate pain, restore motion, and/or correction of previously failed joint replacement procedures, in case where additional component stabilization by means of a stem is required. ii. Co-Cr Hinge Knee – Cemented and iii. Titanium Hinge Knee – Cemented-This Buechel-Pappas Revision Knee Replacement System is intended to provide primary or revision options to the surgeon to correct severe deformity and/or reduce or eliminate pain, restore motion, and/or correction of previously failed joint replacement procedures in the absence of viable collateral ligaments
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Products from the same license holder (10 products)
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Total Knee Replacement System
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Total Hip Replacement System
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Total Knee Replacement System
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About this record

Total Knee Replacement System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000214_34c2e41e8e18584bcde6363d92a64ef3_26bf76ff30bc0a576b551cc5fe2fd4b5. This device is marketed under the brand name Altius. The license holder is TTK HEALTHCARE LIMITED (ORTHO DIVISION), and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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