FDA 510(k) Applications Submitted by ELLIPSE TECHNOLOGIES, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K160325 |
02/05/2016 |
PRECICE Intramedullary Limb Lengthening System |
ELLIPSE TECHNOLOGIES, INC. |
| K140178 |
01/24/2014 |
ELLIPSE MAGEC SPINAL BRACING AND DISTRACTION SYSTEM |
ELLIPSE TECHNOLOGIES, INC. |
| K141278 |
05/16/2014 |
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM |
ELLIPSE TECHNOLOGIES, INC. |
| K131490 |
05/23/2013 |
ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM |
ELLIPSE TECHNOLOGIES, INC. |
| K101997 |
07/15/2010 |
ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM |
ELLIPSE TECHNOLOGIES, INC. |
| K133289 |
10/25/2013 |
PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM |
ELLIPSE TECHNOLOGIES, INC. |
| K113219 |
11/01/2011 |
ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM |
ELLIPSE TECHNOLOGIES, INC. |
| K113695 |
12/16/2011 |
ELLIPSE PRECICE TRAUMA NAIL SYSTEM |
ELLIPSE TECHNOLOGIES, INC. |
| K141023 |
04/21/2014 |
PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM |
ELLIPSE TECHNOLOGIES, INC. |
| K141447 |
06/02/2014 |
PRECICE TRAUMA NAIL SYSTEM |
ELLIPSE TECHNOLOGIES, INC. |
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