NWF

Drill, Battery Powered, Subungual Hematoma

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).

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: NWF
Classification and pathway per current FDA publications. Data from openFDA (CC0).