FZF
- Product code
- FZF
- Device name
- Splint, Extremity, Inflatable, External
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.3900
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 7
Official FDA classification page: FZF
Classification and pathway per current FDA publications. Data from openFDA (CC0).