KWM
- Product code
- KWM
- Device name
- Prosthesis, Wrist, Semi-Constrained
- Device class
- Class 2
- 21 CFR
- 21 CFR 888.3800
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (all years, FDA)
- 6 (all years; only the last 3 years are listed here)
Official FDA classification page: KWM
Classification and pathway per current FDA publications. Data from openFDA (CC0).