KTX
- Product code
- KTX
- Device name
- Prosthesis, Knee, Femorotibial, Non-Constrained, Metal/Composite Cemented
- Device class
- Class 2
- 21 CFR
- 21 CFR 888.3490
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K)
- Flag
- Implant
Official FDA classification page: KTX
Classification and pathway per current FDA publications. Data from openFDA (CC0).