Total shoulder arthroplasty system
FDA product code QHQ · Class 2 · 22 devices · 83 reports · 0 devices named in recalls
- Arthrex® AR-9301-03Arthrex, Inc. · Total shoulder arthroplasty system12 reports
- Arthrex® AR-9301-01Arthrex, Inc. · Total shoulder arthroplasty system9 reports
- Arthrex® AR-9349-18Arthrex, Inc. · Total shoulder arthroplasty system9 reports
- Arthrex® AR-9343-16Arthrex, Inc. · Total shoulder arthroplasty system7 reports
- Arthrex® AR-9347-18Arthrex, Inc. · Total shoulder arthroplasty system7 reports
- Arthrex® AR-9301-02Arthrex, Inc. · Total shoulder arthroplasty system6 reports
- Arthrex® AR-9345-17Arthrex, Inc. · Total shoulder arthroplasty system6 reports
- Arthrex® AR-9341-16Arthrex, Inc. · Total shoulder arthroplasty system5 reports
- Arthrex® AR-9301-43CPCArthrex, Inc. · Total shoulder arthroplasty system3 reports
- Arthrex® AR-9301-45CPCArthrex, Inc. · Total shoulder arthroplasty system3 reports
- Arthrex® AR-9301-47CPCArthrex, Inc. · Total shoulder arthroplasty system3 reports
- Arthrex® AR-9339-18Arthrex, Inc. · Total shoulder arthroplasty system2 reports
- Arthrex® AR-9301-39CPCArthrex, Inc. · Total shoulder arthroplasty system2 reports
- Arthrex® AR-9300-43CPCArthrex, Inc. · Total shoulder arthroplasty system1 report
- Arthrex® AR-9300-49CPCArthrex, Inc. · Total shoulder arthroplasty system1 report
- Arthrex® AR-9301-04Arthrex, Inc. · Total shoulder arthroplasty system1 report
- Arthrex® AR-9339-16Arthrex, Inc. · Total shoulder arthroplasty system1 report
- Arthrex® AR-9347-20Arthrex, Inc. · Total shoulder arthroplasty system1 report
- Arthrex® AR-9349-20Arthrex, Inc. · Total shoulder arthroplasty system1 report
- Arthrex® AR-9351-19Arthrex, Inc. · Total shoulder arthroplasty system1 report
- Arthrex® AR-9301-49CPCArthrex, Inc. · Total shoulder arthroplasty system1 report
- Arthrex® AR-9301-51CPCArthrex, Inc. · Total shoulder arthroplasty system1 report