KYK
- Product code
- KYK
- Device name
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Composite
- Device class
- Class 2
- 21 CFR
- 21 CFR 888.3500
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (last 3 years)
- 3
Official FDA classification page: KYK
Classification and pathway per current FDA publications. Data from openFDA (CC0).