KXE
- Product code
- KXE
- Device name
- Prosthesis, Wrist, Hemi-, Ulnar
- Device class
- Class 2
- 21 CFR
- 21 CFR 888.3810
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (last 3 years)
- 16
Official FDA classification page: KXE
Classification and pathway per current FDA publications. Data from openFDA (CC0).