spinal channeling instrument, vertebroplasty

FDA product code OCJ · Class 1 · 3 devices · 14 reports · 0 devices named in recalls

• NA 0306621000

  Stryker Corporation · spinal channeling instrument, vertebroplasty
  11 reports
• NA 0306620000

  Stryker Corporation · spinal channeling instrument, vertebroplasty
  2 reports
• OptaBlate 9700811000

  Stryker Corporation · spinal channeling instrument, vertebroplasty
  1 report