ArthroCare Medical Corporation
5 FDA 510(k) clearances · Recalling firm
◉ Watch ArthroCare Medical Corporation
| Record | Firm | Date |
|---|---|---|
| EVAC 70 XTRA with Integrated Cable REF EICA5872-01 Product Usage: PLASMA WAND devices are recall (Z-1832-2015) | ArthroCare Medical Corporation | 2015-06-25 |
| PROcise XP Wand with Integrated Cable REF EICA8872-01 Product Usage: PLASMA WAND devices a recall (Z-1833-2015) | ArthroCare Medical Corporation | 2015-06-25 |
| Coblator II System, 120V. Product Usage: The Coblator II (Model RF8000E) is a bipolar, rad recall (Z-1323-2015) | ArthroCare Medical Corporation | 2015-03-26 |
| Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger Switches and Model recall (Z-0579-2015) | ArthroCare Medical Corporation | 2014-12-16 |
| Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-ST recall (Z-0652-2014) | ArthroCare Medical Corporation | 2014-01-09 |
Track ArthroCare Medical Corporation automatically
Every clearance here is in the API, with alerts when new ones post.