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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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