Hydrocision, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
FDA 510(k) cleared devices by Hydrocision, Inc. Orthopedic ✕
8 devices
Cleared
Jul 30, 2025
SpineSite Endoscope System
Orthopedic
387d
Cleared
Apr 16, 2020
HydroCision SpineJet System
Orthopedic
27d
Cleared
Jul 28, 2004
ARTHROJET XT
Orthopedic
79d
Cleared
Sep 16, 2003
HYDROCISION ARTHROJET SYSTEM WITH CAUTERY, TURBOBURR AND CURETTE, MODELS...
Orthopedic
32d
Cleared
Apr 03, 2002
HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR
Orthopedic
30d
Cleared
Nov 24, 2000
HYDROCISION ARTHROJET SYSTEM WITH CAUTERY AND BURR
Orthopedic
80d
Cleared
Oct 25, 1999
HYDROCISION ARTHROJET SYSTEM WITH CAUTERY
Orthopedic
48d
Cleared
Sep 25, 1998
HYDROCISION ARTHROJET SYSTEM
Orthopedic
88d