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FDA 510(k) Applications Submitted by John McIntyre
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140178
01/24/2014
ELLIPSE MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
ELLIPSE TECHNOLOGIES, INC.
K140613
03/10/2014
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.
K131677
06/10/2013
PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
ELLIPSE TECHNOLOGIES INC.
K101997
07/15/2010
ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
ELLIPSE TECHNOLOGIES, INC.
K152370
08/21/2015
PRECICE Trauma Nail System
Ellipse Technologies Incorporated
K133289
10/25/2013
PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
ELLIPSE TECHNOLOGIES, INC.
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