KWF
- Product code
- KWF
- Device name
- Prosthesis, Finger, Polymer
- Device class
- Class 2
- 21 CFR
- 21 CFR 888.3230
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K)
- Flag
- Implant
Official FDA classification page: KWF
Classification and pathway per current FDA publications. Data from openFDA (CC0).