MPI — Glenoid Fossa Prosthesis Class III

FDA Device Classification

FDA product code MPI covers "Glenoid Fossa Prosthesis", a Class III medical device regulated under 21 CFR 872.3950. Submissions are reviewed by the Dental panel. Devices under this code are implants.

Classification Details

Product Code
MPI
Device Class
Class III
Regulation Number
872.3950
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
Yes