Implants International, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 2
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K132539 | RING-LOK MODULAR BIPOLAR SYSTEM | February 7, 2014 |
| K071583 | CERMET III ACETABULAR CUP SYSTEM | July 25, 2007 |