NFS — Device, Jaw Tracking, For Monitoring Jaw Positions Class I

FDA Device Classification

FDA product code NFS covers "Device, Jaw Tracking, For Monitoring Jaw Positions", a Class I medical device regulated under 21 CFR 872.2060. Submissions are reviewed by the Dental panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
NFS
Device Class
Class I
Regulation Number
872.2060
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K952218bio-research associatesJT-3 ELECTROGNATHOGRAPHSeptember 21, 1995
K843951siemens medical solutions usaSIROGNATHOGRAPHNovember 14, 1984