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CDSCO UID IMP/MD/2019/000496_c0aa1ca53a245f19a42149602a09a398_ad15cff11158295625dbd201b0feb90d

Total Hip replacement system

M/s Stryker India Private Ltd.,·Device Class Class C·India CDSCO·Brand: Femoral Stems
Registration details
UID
IMP/MD/2019/000496_c0aa1ca53a245f19a42149602a09a398_ad15cff11158295625dbd201b0feb90d
Device class
Class C
Brand name
Femoral Stems
License holder
M/s Stryker India Private Ltd.,
Approving authority
CDSCO
Product information
The indications for use for total hip and hemi hip arthroplasty include: 1. Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis; 2. rheumatoid arthritis; 3. correction of functional deformity; 4. revision procedures where other treatments or devices have failed; and, 5. treatment of nonunion, femoral neck and trochanteric fractures of the proximal femur with head involvement that are unmanageable using other techniques
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About this record

Total Hip replacement system is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000496_c0aa1ca53a245f19a42149602a09a398_ad15cff11158295625dbd201b0feb90d. This device is marketed under the brand name Femoral Stems. The license holder is M/s Stryker India Private Ltd.,, and it is classified as Device Class Class C. The approving authority is CDSCO.

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