Medical Device Manufacturer · GB , Harrogate, North Yorkshire

Arthocare Corporation - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2001
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arthocare Corporation Orthopedic ✕
3 devices
1-3 of 3
Cleared Jan 19, 2016
MultiFIX S Ultra Knotless Fixation System
K153669 · MBI
Orthopedic · 29d
Cleared Jul 29, 2013
MULTIFIX S KNOTLESS FIXATION DEVICE
K131182 · MBI
Orthopedic · 94d
Cleared Dec 13, 2001
ENDOFLIP
K013334 · MBI
Orthopedic · 65d
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All6 General & Plastic Surgery 3 Orthopedic 3