Retention Device, Suture

FDA product code KGS · Class 1 · 3 devices · 7 reports · 1 devices named in recalls

• Q-Stop QS

  DRS Vascular, Inc. · Retention Device, Suture
  1 recall0 reports
• XTENDOBUTTON 71935602

  Smith & Nephew, Inc. · RETENTION DEVICE, SUTURE
  5 reports
• XTENDOBUTTON 72200134

  Smith & Nephew, Inc. · RETENTION DEVICE, SUTURE
  2 reports