510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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NWFClass I

Drill, Battery Powered, Subungual Hematoma

21 CFR 878.4820 / General, Plastic Surgery
FDA source (opens on fda.gov)

NWF is the FDA product code for Drill, Battery Powered, Subungual Hematoma, a class I device type, regulated under 21 CFR 878.4820. FDA's definition for this code reads: "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)". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
NWF
Device name
Drill, Battery Powered, Subungual Hematoma
FDA 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).
Regulation
21 CFR 878.4820
Device class
Class I
Review panel
General, Plastic Surgery
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code NWF

By decision year
1 clearance under product code NWF with a decision year between 2005 and 2005, 2005 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NWF by decision year
YearClearances
20051

Applicants with the most clearances

Product code NWF
Applicants holding the most 510(k) clearances under product code NWF
ApplicantClearances
Path Scientific1

Companies listing this code with FDA

Companies whose registered establishments list this code