Cochlear Bone Anchored Systems AB
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K090720 | COCHLEAR BAHA BP100 | June 17, 2009 |
| K080363 | BAHA CORDELLE II | April 10, 2008 |