In Brief: Dental Products Panel
This article was originally published in The Gray Sheet
Executive Summary
Dental Products Panel: Review of a premarket approval application for a bone filling/augmentation device is on the agenda for a Jan. 12 meeting at FDA's Corporate Building in Rockville, Maryland. On Jan. 13, the panel will focus on the appropriate classification of the following endosseous implant subgroups: coated and uncoated root form implants, coated and uncoated blade-type implants, temporary implants, and implants with special enhanced features. Written submissions are due at the agency by Dec. 29; for more information contact FDA's Pamela Scott at 301/827-5283...