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Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Composite

FDA product code KYK · 3 cleared devices

Class 2 Orthopedic
Regulation
21 CFR 888.3500
Review panel
OR
Implant
Yes
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1985-07-15 – 1988-03-14
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