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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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