NWF
- Product code
- NWF
- Device name
- Drill, Battery Powered, Subungual Hematoma
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.4820
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 1 (all years; only the last 3 years are listed here)
FDA classification definition
Intended to cut a hole in finger and toe nails to release fluid accumulated in the underlying nail bed. Indicated to relieve pressure from subungual hematomas (including black toe).
Official FDA classification page: NWF
Classification and pathway per current FDA publications. Data from openFDA (CC0).