Bone Wedge
FDA product code PLF · Class 2 · 8 devices · 3 reports · 5 devices named in recalls
- Arthrex® AR-8948W-1665Arthrex, Inc. · Bone Wedge2 recalls0 reports
- Arthrex® AR-8948W-1645Arthrex, Inc. · Bone Wedge1 recall0 reports
- Arthrex® AR-8948W-2045Arthrex, Inc. · Bone Wedge1 recall0 reports
- Arthrex® AR-8948W-2055Arthrex, Inc. · Bone Wedge1 recall0 reports
- Arthrex® AR-8948W-2065Arthrex, Inc. · Bone Wedge1 recall0 reports
- Arthrex® AR-8942W-1806Arthrex, Inc. · Bone Wedge1 report
- Arthrex® AR-8942W-2006Arthrex, Inc. · Bone Wedge1 report
- Arthrex® AR-8948W-2075Arthrex, Inc. · Bone Wedge1 report