Product code GDN— General, Plastic Surgery
9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS
- Classification name
- Knife, Amputation
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code GDN
FDA has cleared device under product code GDN, all in 1985, filed by 1 applicant company. 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.
Top applicants under product code GDN
Recent clearances under product code GDN
Data sourced from openFDA. This site is unofficial and independent of the FDA.