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Renovis Surgical Technologies

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories5
Latest Approval2019-06-20
TypeNumberDevice NameCodeDate
510(k) K190122 Renovis A200 PS Knee System as part of the Renovis A200 Knee System JWH 2019-06-20 View
510(k) K182007 Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System OVD 2018-12-07 View
510(k) K181655 Renovis S180 Lateral Lumbar Interbody Fusion System MAX 2018-09-11 View
510(k) K171543 Renovis Surgical Hip Replacement System OQG 2017-11-16 View
510(k) K170888 Renovis S141 Lumbar Interbody Fusion System MAX 2017-08-08 View
510(k) K153250 Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System OVE 2016-03-16 View