KBX
- Product code
- KBX
- Device name
- Screw, Tonsil
- Device class
- Class 1
- 21 CFR
- 21 CFR 874.4420
- Medical specialty
- Ear, Nose, Throat
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: KBX
Classification and pathway per current FDA publications. Data from openFDA (CC0).