Vertebral body tethering system

FDA product code QHP · Class N · 12 devices · 59 reports · 0 devices named in recalls

• The Tether™ 204H0300

  Zimmer Biomet Inc · Vertebral Body Tethering System
  29 reports
• The Tether™ 211H6032

  Zimmer Biomet Inc · Vertebral Body Tethering System
  6 reports
• The Tether™ 203H0012

  Zimmer Biomet Inc · Vertebral Body Tethering System
  6 reports
• The Tether™ 211H6030

  Zimmer Biomet Inc · Vertebral Body Tethering System
  4 reports
• The Tether™ 211H6035

  Zimmer Biomet Inc · Vertebral Body Tethering System
  3 reports
• The Tether™ 211H6040

  Zimmer Biomet Inc · Vertebral Body Tethering System
  2 reports
• The Tether™ 211H7035

  Zimmer Biomet Inc · Vertebral Body Tethering System
  2 reports
• The Tether™ 211H7037

  Zimmer Biomet Inc · Vertebral Body Tethering System
  2 reports
• The Tether™ 211H7040

  Zimmer Biomet Inc · Vertebral Body Tethering System
  2 reports
• REFLECT 1244.1250S

  Globus Medical, Inc. · Vertebral body tethering system
  1 report
• REFLECT 1244.1351S

  Globus Medical, Inc. · Vertebral body tethering system
  1 report
• The Tether™ 211H6025

  Zimmer Biomet Inc · Vertebral Body Tethering System
  1 report