Spinefrontier, Inc.

4 devices · 7 adverse event reports · 0 devices named in recalls

Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.

• PedFuse® 01-80101

  ORTHOSIS, SPINAL PEDICLE FIXATION
  3 reports
• Indus® IM71059-03

  APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
  2 reports
• A-CIFT® SoloFuse® 01-32017-06

  Intervertebral fusion device with integrated fixation, cervical
  1 report
• PedFuse 01-80325

  Orthosis, spinal pedicle fixation
  1 report