American Design Group, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K911717 | ADG INTRAMEDULLARY BONE PLUG - VENTED | September 4, 1991 |
| K902615 | ADG BONE PLUG | September 11, 1990 |
| K890722 | ADG BONE BIOPSY SYSTEM | September 21, 1989 |