FDA 510(k) Applications Submitted by ELLIPSE TECHNOLOGIES INC.

FDA 510(k) Number Submission Date Device Name Applicant
K140613 03/10/2014 MAGEC SPINAL BRACING AND DISTRACTION SYSTEM ELLIPSE TECHNOLOGIES INC.
K131677 06/10/2013 PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM ELLIPSE TECHNOLOGIES INC.
K141739 06/27/2014 RESIDUAL LIMB LENGTHENING SYSTEM ELLIPSE TECHNOLOGIES INC.


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