Ellipse Technologies, Incorporated
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K160267 | PRECICE Trauma Nail System | March 31, 2016 |
| K151594 | Ellipse Supplemental Instrument Trays | January 25, 2016 |
| K152370 | PRECICE Trauma Nail System | December 22, 2015 |
| K151131 | PRECICE Intramedullary Limb Lengthening System | June 19, 2015 |
| K150885 | MAGEC 2 Spinal Bracing and Distraction System | May 29, 2015 |
| K150656 | PRECICE Intramedullary Limb Lengthening System | April 23, 2015 |
| K142599 | PRECISE Trauma Nail System | January 16, 2015 |