Shoulder arthroplasty implantation system

FDA product code QHE · Class 2 · 6 devices · 4 reports · 3 devices named in recalls

• CORE Shoulder System 87-9136

  Link Bio Corp · Shoulder Arthroplasty Implantation System
  1 recall1 report
• Blueprint BPUE001

  Tornier · Shoulder arthroplasty implantation system
  1 recall0 reports
• Blueprint BPUE001

  Tornier · Shoulder arthroplasty implantation system
  1 recall0 reports
• Arthrex® 5566VIP

  Arthrex, Inc. · Shoulder arthroplasty implantation system
  1 report
• Comprehensive® Reverse Shoulder Augmented Guide and Bone Model Left 20-8090-004-01

  Orthosoft Inc · Shoulder Arthroplasty Implantation System
  1 report
• Comprehensive® Reverse Shoulder Augmented Guide and Bone Model Right 20-8090-004-02

  Orthosoft Inc · Shoulder Arthroplasty Implantation System
  1 report