NWF · Class I · 21 CFR 878.4820

FDA Product Code NWF: Drill, Battery Powered, Subungual Hematoma

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).

Leading manufacturers include Path Scientific, LLC.

Total

Cleared

31d

Avg days

2005

Since

FDA 510(k) Cleared Drill, Battery Powered, Subungual Hematoma Devices (Product Code NWF)

1 devices

1–1 of 1

General & Plastic Surgery · 31d

About Product Code NWF - Regulatory Context

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Data Source

FDA 510(k) public files . 176,583 total devices indexed.

Latest clearance: Oct 31, 2005

Product Code Info

Code	NWF
Device class	Class I
CFR	21 CFR 878.4820
Panel	General & Plastic Surgery

Verify on FDA.gov

View NWF classification on FDA.gov →