Arthocare Corporation - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Arthocare Corporation has 6 FDA 510(k) cleared medical devices. Based in Harrogate, North Yorkshire, GB.
Historical record: 6 cleared submissions from 2001 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Arthocare Corporation Filter by specialty or product code using the sidebar.
6 devices
Cleared
Jan 19, 2016
MultiFIX S Ultra Knotless Fixation System
Orthopedic
29d
Cleared
Jul 29, 2013
MULTIFIX S KNOTLESS FIXATION DEVICE
Orthopedic
94d
Cleared
Dec 11, 2012
AMBIENT TURBOFLASH 90 IFS
General & Plastic Surgery
271d
Cleared
Nov 07, 2012
SMARTSTITCH PERFECTPASSER SYSTEM
General & Plastic Surgery
19d
Cleared
Jul 12, 2012
SMARTSTITCH M-CONNECTOR ULTRA SMARTSTITCH SUTURE DEVICE HANDLE SMARTSTITCH...
General & Plastic Surgery
72d
Cleared
Dec 13, 2001
ENDOFLIP
Orthopedic
65d