HWD
- Product code
- HWD
- Device name
- Starter, Bone Screw
- Device class
- Class 1
- 21 CFR
- 21 CFR 888.4540
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: HWD
Classification and pathway per current FDA publications. Data from openFDA (CC0).