HBD — Handpiece (Brace), Drill Class I

FDA Device Classification

FDA product code HBD covers "Handpiece (Brace), Drill", a Class I medical device regulated under 21 CFR 882.4325. Submissions are reviewed by the Neurology panel.

Classification Details

Product Code
HBD
Device Class
Class I
Regulation Number
882.4325
Submission Type
Review Panel
NE
Medical Specialty
Neurology
Implant
No