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

Saw, Electrically Powered

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

DWI is the FDA product code for Saw, Electrically Powered, a class I device type, regulated under 21 CFR 878.4820. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DWI
Device name
Saw, Electrically Powered
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
2
Ingested recalls
0

Clearances, product code DWI

By decision year
2 clearances under product code DWI with a decision year between 1980 and 1991, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DWI by decision year
YearClearances
19801
19911

Applicants with the most clearances

Product code DWI
Applicants holding the most 510(k) clearances under product code DWI
ApplicantClearances
Stryker Medical1
Temp Medical Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 15 companies shown, in name order