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CDSCO UID IMP/MD/2019/000423_7072a2ec406889934f333b6a18d3cb62_9aef46acae2aa36a532fb424b4b896d6

CR-PS Knee System - Femoal

Johnson & Johnson Private Limited·Device Class Class D·India CDSCO·Brand: PFC Sigma
Registration details
UID
IMP/MD/2019/000423_7072a2ec406889934f333b6a18d3cb62_9aef46acae2aa36a532fb424b4b896d6
Device class
Class D
Brand name
PFC Sigma
License holder
Johnson & Johnson Private Limited
Approving authority
CDSCO
Product information
It is Indicated for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis, rheumatoid arthritis, or a failed previous implant
Similar products (4)
Other products with the same name or brand
Knee System - Stem
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CR-PS Knee System - Inserts
Brand: PFC Sigma
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About this record

CR-PS Knee System - Femoal is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000423_7072a2ec406889934f333b6a18d3cb62_9aef46acae2aa36a532fb424b4b896d6. This device is marketed under the brand name PFC Sigma. 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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