Arrowhead Medical Device Technologies, LLC
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K180539 | Deformity Analysis and Correction Software (DACS) and Instrumentation | August 13, 2018 |
| K112675 | ARROW-LOK DIGITAL SYSTEM | December 12, 2011 |