Product code HXS— Orthopedic
FLAT WRENCH
- Classification name
- Twister, Wire
- Device class
- Class 1
- Regulation
- 21 CFR 888.4540
- Advisory panel
- Orthopedic
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code HXS
FDA has cleared devices under product code HXS between 1978 and 1983, 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
- 1983
- 1978
Top applicants under product code HXS
Recent clearances under product code HXS
Data sourced from openFDA. This site is unofficial and independent of the FDA.