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U&I Corporation

FDA 510(k) & PMA Approved Devices — 16 products

Total Devices16
Categories9
Latest FDA decision2022-02-16
TypeNumberDevice NameCodeDateActions
510(k) K220147 Aspiron S ACP SystemKWQ2022-02-16 View
510(k) K210573 Velofix SA Cervical CageOVE2021-11-19 View
510(k) K183243 Velofix TLIF CageMAX2019-07-10 View
510(k) K190067 Velofix Interbody Fusion SystemODP2019-02-04 View
510(k) K190053 SECULOK™ ACP SystemKWQ2019-02-01 View
510(k) K181824 CBT Screw Fixation SystemNKB2018-12-13 View
510(k) K183383 ANAX™ OCT Spinal SystemNKG2018-12-12 View
510(k) K181829 Velofix TLIF CageMAX2018-11-14 View
510(k) K182055 SECULOK™ ACP SystemKWQ2018-09-10 View
510(k) K180759 SECULOK™ Suture AnchorMBI2018-08-09 View
510(k) K173198 Facet Screw Fixation SystemMRW2018-01-03 View
510(k) K173524 ANAX 5.5™ Spinal SystemNKB2017-12-13 View
510(k) K172419 Velofix™ TLIF CageMAX2017-12-04 View
510(k) K172424 Velofix™ SA Cervical CageOVE2017-11-22 View
510(k) K171749 Velofix(tm) Interbody Fusion SystemODP2017-07-13 View
510(k) K162189 ANAX™ 5.5 Spinal SystemMNH2016-08-30 View
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