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Dio Medical Corporation

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories4
Latest FDA decision2022-10-25
TypeNumberDevice NameCodeDateActions
510(k) K222415 Rexious Spinal Fixation SystemNKB2022-10-25 View
510(k) K222572 FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, and BALTEUM™ & BALTEUM-ONE™ Lumbar Plate SystemKWQ2022-10-18 View
510(k) K222448 UNITY Sacroiliac Joint Fixation SystemOUR2022-10-13 View
510(k) K222515 FaSet Fixation SystemMRW2022-10-05 View
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