KDA
- Product code
- KDA
- Device name
- Prosthesis, Ptfe/Carbon-Fiber
- Device class
- Class 2
- 21 CFR
- 21 CFR 878.3500
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (last 3 years)
- 1
Official FDA classification page: KDA
Classification and pathway per current FDA publications. Data from openFDA (CC0).