FDA 510(k) Applications Submitted by Ellipse Technologies, Incorporated

FDA 510(k) Number Submission Date Device Name Applicant
K160267 02/02/2016 PRECICE Trauma Nail System Ellipse Technologies, Incorporated
K151594 06/12/2015 Ellipse Supplemental Instrument Trays Ellipse Technologies, Incorporated
K150656 03/13/2015 PRECICE Intramedullary Limb Lengthening System Ellipse Technologies, Incorporated
K150885 04/02/2015 MAGEC 2 Spinal Bracing and Distraction System Ellipse Technologies, Incorporated
K151131 04/28/2015 PRECICE Intramedullary Limb Lengthening System Ellipse Technologies, Incorporated
K142599 09/15/2014 PRECISE Trauma Nail System Ellipse Technologies, Incorporated


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