Stuckenbrock Medizintechnik GmbH
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K171624 | IXOS Radius Plate System | March 29, 2018 |
| K171628 | HBS2 Headless Bone Screw | January 12, 2018 |
| K042902 | HERBERT ULNAR HEAD PROSTHESIS SYSTEM | December 27, 2004 |