Product code HXG— Orthopedic
PUNCH
- Classification name
- Tamp
- Device class
- Class 1
- Regulation
- 21 CFR 888.4540
- Advisory panel
- Orthopedic
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code HXG
FDA has cleared device under product code HXG, all in 1984, 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 HXG
Recent clearances under product code HXG
Data sourced from openFDA. This site is unofficial and independent of the FDA.