KFX · Class II · 21 CFR 890.3500

FDA Product Code KFX: Assembly, Thigh/knee/shank/ankle/foot, External

4
Total
4
Cleared
74d
Avg days
1982
Since

FDA 510(k) Cleared Assembly, Thigh/knee/shank/ankle/foot, External Devices (Product Code KFX)

4 devices
1–4 of 4
No devices found for this product code.

About Product Code KFX - Regulatory Context