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FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest Approval2025-07-18
TypeNumberDevice NameCodeDate
510(k) K243775 True Non-Surgical Spinal Decompression System (DRX9000-SL) ITH 2025-07-18 View
510(k) K243366 DRX9000C-SL Cervical Spinal Decompression System ITH 2025-06-18 View
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