FDA 510(k) Applications Submitted by Ortho Development Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K182085 08/02/2018 Balanced Knee Revision System Trabecular Tibial Cone Augments Ortho Development Corporation
K180743 03/22/2018 Balanced Knee Revision System - Offset Junction Box Ortho Development Corporation
K181569 06/14/2018 BKS Revision Sleeves System Ortho Development Corporation
K200281 02/04/2020 The Gecko Spinal System Ortho Development Corporation
K211086 04/12/2021 The ProgenÖ Trochanteric Nail System Ortho Development Corporation
K211471 05/11/2021 Balanced Knee System Uni Ortho Development Corporation
K203023 10/02/2020 Pisces Spinal System Ortho Development Corporation
K161080 04/18/2016 Escalade Legend Acetabular Shell ORTHO DEVELOPMENT CORPORATION
K171249 04/28/2017 EntradaÖ hip stem Ortho Development Corporation
K152169 08/04/2015 Balanced Knee System TriMax CR Femoral Component and E-Vitalize CR and UC Tibial Inserts ORTHO DEVELOPMENT CORPORATION
K153216 11/05/2015 Alpine Cemented Hip System ORTHO DEVELOPMENT CORPORATION
K173951 12/27/2017 Legend Acetabular Liners Ortho Development Corporation
K162995 10/27/2016 Ibis« Pedicle Screw System Ortho Development Corporation


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