Knee Replacement System - Patella -
- UID
- IMP/MD/2019/000489_788c2808247df26bb2c5f8a7f89170ab_c0faf3a40ef3c52208e1bbe6e177be8c
- Device class
- Class D
- Brand name
- Global Advantage - Head
- License holder
- Johnson & Johnson Private Limited
- 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, posttraumatic arthritis, collagen disorders, or pseudo gout. 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.
Knee Replacement System - Patella - is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000489_788c2808247df26bb2c5f8a7f89170ab_c0faf3a40ef3c52208e1bbe6e177be8c. 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.