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Hydrocision, Inc.

FDA 510(k) & PMA Approved Devices — 12 products

Total Devices12
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K241990 SpineSite Endoscope SystemHRX2025-07-30 View
510(k) K200729 HydroCision SpineJet SystemHRX2020-04-16 View
510(k) K190804 HydroCision TenJet DeviceHRX2019-06-05 View
510(k) K041233 ARTHROJET XTHRX2004-07-28 View
510(k) K032529 HYDROCISION ARTHROJET SYSTEM WITH CAUTERY, TURBOBURR AND CURETTE, MODELS 51300, 51310HRX2003-09-16 View
510(k) K021813 HYDROCISION GENERAL SURGERY FLUIDJET SYSTEMFQH2003-05-09 View
510(k) K020688 HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURRHRX2002-04-03 View
510(k) K011612 MODIFICATION TO HYDROCISION DEBRIDEMENT SYSTEMFQH2001-06-22 View
510(k) K002764 HYDROCISION ARTHROJET SYSTEM WITH CAUTERY AND BURRHRX2000-11-24 View
510(k) K991383 HYDROCISION DEBDRIDEMENT SYSTEMFQH2000-03-31 View
510(k) K993009 HYDROCISION ARTHROJET SYSTEM WITH CAUTERYHRX1999-10-25 View
510(k) K982266 HYDROCISION ARTHROJET SYSTEMHRX1998-09-25 View
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