FDA 510(k) Applications Submitted by William W. Sowers

FDA 510(k) Number Submission Date Device Name Applicant
K130317 02/08/2013 GENESYS SPINE APACHE IBFD STAR CERVICAL SYSTEM GENESYS SPINE
K130913 04/02/2013 GENESYS SPINE APACHE LATERAL LUMBAR INTERBODY FUSION SYSTEM GENESYS SPINE
K152039 07/22/2015 Genesys Spine TiLock2 Spinal System Genesys Spine
K133245 10/22/2013 GENESYS SPINE ANTERIOR CERVICAL PLATE II SYSTEM GENESYS SPINE
K171838 06/20/2017 TiLock2 Spinal System Genesys Spine
K191748 07/01/2019 Genesys Spine Sacroiliac Joint Fusion System Genesys Spine
K161914 07/12/2016 Genesys Spine TiLock Cortical Spinal System Genesys Spine
K182987 10/29/2018 Genesys Spine 3DP Lumbar Interbody System Genesys Spine


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