GFB
- Product code
- GFB
- Device name
- Head, Surgical, Hammer
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.4820
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: GFB
Classification and pathway per current FDA publications. Data from openFDA (CC0).