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FYI — Appliance, Facial Fracture, External Class I

FDA Device Classification

Classification Details

Product Code
FYI
Device Class
Class I
Regulation Number
878.3250
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K871073omega siliconeOMEGA BIVALVE NASAL SPLINTSMay 11, 1987
K821178ethiconETHICON EXTERNAL FIXATION WIREJune 11, 1983
K801072surgical technology laboratoriesSTRAITH NASAL SPLINTJune 17, 1980
K792106conpharCONPHAR O.R. HEAD COVER-STERILENovember 5, 1979