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 General & Plastic Surgery ✕
3 devices
1-3 of 3
Cleared Dec 11, 2012
AMBIENT TURBOFLASH 90 IFS
K120791 · GEI
General & Plastic Surgery · 271d
Cleared Nov 07, 2012
SMARTSTITCH PERFECTPASSER SYSTEM
K123268 · GAT
General & Plastic Surgery · 19d
Cleared Jul 12, 2012
SMARTSTITCH M-CONNECTOR ULTRA SMARTSTITCH SUTURE DEVICE HANDLE SMARTSTITCH...
K121306 · GAT
General & Plastic Surgery · 72d
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