KFX
- Product code
- KFX
- Device name
- Assembly, Thigh/Knee/Shank/Ankle/Foot, External
- Device class
- Class 2
- 21 CFR
- 21 CFR 890.3500
- Medical specialty
- Physical Medicine
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 4 (all years; only the last 3 years are listed here)
Official FDA classification page: KFX
Classification and pathway per current FDA publications. Data from openFDA (CC0).