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Knee Replacement System - India CDSCO Medical Device Registration

Knee Replacement System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000489_b4cbdc2f894bdfc899874a16beba1031_986f4937af5cdb69c01a969220e43eca. This device is marketed under the brand name Global Advantage - Head. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class D
Knee Replacement System
UID: IMP/MD/2019/000489_b4cbdc2f894bdfc899874a16beba1031_986f4937af5cdb69c01a969220e43eca

Brand Name

Global Advantage - Head

Device Class

Class D

Approving Authority

CDSCO

Product Information

The P.F.C. SIGMA and P.F.C. Modular Knee System — Patella components are indicated for use in knee replacements for patients suffering from severe pain and disability due to permanent structural damage in the knee joint from rheumatoid arthritis, osteoarthritis, post-traumatic arthritis, collagen disorders, or pseudogout. This damage may also be the result of trauma or failed prior surgical intervention. The P.F.C. SIGMA and P.F.C. Modular Knee System — Patella components are indicated for use only with PMMA bone cement

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