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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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