Product code HWM— General, Plastic Surgery
ACROMED WALLIE-HEINIG OSTEOTOMES
- Classification name
- Osteotome
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code HWM
FDA has cleared devices under product code HWM between 1977 and 1987, filed by 3 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
- 1987
- 1977
Top applicants under product code HWM
Adverse events under product code HWM
product code HWM- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code HWM
Data sourced from openFDA. This site is unofficial and independent of the FDA.