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Ldr Spine USA, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories3
Latest FDA decision2017-05-16
TypeNumberDevice NameCodeDateActions
510(k) K162133 VerteFIT Corpectomy Cage SystemMQP2017-05-16 View
510(k) K161173 Avenue® T TLIF CageOVD2016-09-28 View
510(k) K161798 FacetBRIDGE® SystemMRW2016-08-04 View