Manual instruments designed for use with total disc replacement devices

FDA product code QLQ · Class 2 · 2 devices · 6 reports · 0 devices named in recalls

• activL® FW961R

  Aesculap AG · Manual instruments designed for use with total disc replacement devices
  4 reports
• activL® FW965R

  Aesculap AG · Manual instruments designed for use with total disc replacement devices
  2 reports