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Patella – - India CDSCO Medical Device Registration

Patella – is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000112_dbef666829a4f7b7af96de9fdaf4f2c9_053cf3b4dec4b0943da65f010938aa62. This device is marketed under the brand name Total Knee Replacement. The license holder is Stryker India Pvt. Ltd.,, and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered
Class Class C
Patella –
UID: IMP/MD/2020/000112_dbef666829a4f7b7af96de9fdaf4f2c9_053cf3b4dec4b0943da65f010938aa62

Brand Name

Total Knee Replacement

Device Class

Class C

Approving Authority

CDSCO

Product Information

It is indicated in painful ,disabling joint disease of the Knee resulting from degenerative arthritis rheumatoid arthritis or post-traumatic arthritis, post traumatic loss of knee joint configuration and function , moderate varus , valgus ,or flexion deformity in which the ligamentous structures can be returned to adequate function and stability, revision of previous unsuccessful Knee replacement or other procedure,: Augments , Blocks Stems, Plugs, Offset adaptors, Extensions, Screws

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