Product code GDR— General, Plastic Surgery

27-100 TO 29-130 VARIOUS BONE SAWS-CHARRIERE, SATT

Classification name
Saw, Manual And Accessories
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
2
First cleared
Most recent

Market context for product code GDR

FDA has cleared 2 devices under product code GDR between 1985 and 1987, filed by 2 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

Top applicants under product code GDR

Recent clearances under product code GDR

Data sourced from openFDA. This site is unofficial and independent of the FDA.