HXW
- Product code
- HXW
- Device name
- Bender
- Device class
- Class 1
- 21 CFR
- 21 CFR 888.4540
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 3
Official FDA classification page: HXW
Classification and pathway per current FDA publications. Data from openFDA (CC0).