Knee Replacement System-Femoral - India CDSCO Medical Device Registration

Knee Replacement System-Femoral is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000029_ea8ef357146176f952d311ecdb7ac72b_6425bcfc13e3925e4052f50e0fe0f970. This device is marketed under the brand name LPS. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.

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CDSCO Registered

Class Class D

Knee Replacement System-Femoral

UID: IMP/MD/2019/000029_ea8ef357146176f952d311ecdb7ac72b_6425bcfc13e3925e4052f50e0fe0f970

Brand Name

LPS

License Holder

Johnson & Johnson Private Limited

Device Class

Class D

Approving Authority

CDSCO

Product Information

Sigma Knee System intended to provide increased patient mobility and reduced pain by replacing the damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. Total or unicompartmental knee replacement may be considered for younger patients if, in the opinion of the surgeon, an unequivocal indication for total or unicompartmental knee replacement outweighs the risks associated with the age of the patient, and if limited demands regarding activity and knee jointloading can be assured. This includes severely crippled patients with multiple joint involvement for whom a gain in knee mobility may lead to an expectation of significant improvement in the quality of their lives

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Knee Replacement System-Femoral

Brand: Sigma PS

Johnson & Johnson Private Limited

Knee Replacement System-Femoral - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

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