Ellipse Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K160325 | PRECICE Intramedullary Limb Lengthening System | HSB | 2016-04-04 | View |
| 510(k) | K133289 | PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM | HSB | 2013-12-09 | View |
| 510(k) | K131677 | PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM | HSB | 2013-10-11 | View |
| 510(k) | K113219 | ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM | HSB | 2012-10-19 | View |
| 510(k) | K113695 | ELLIPSE PRECICE TRAUMA NAIL SYSTEM | HSB | 2012-03-28 | View |
| 510(k) | K101997 | ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM | HSB | 2011-07-12 | View |
No matching devices.
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