Knee arthroplasty implantation system

FDA product code OOG · Class 2 · 14 devices · 429 reports · 0 devices named in recalls

• iTotal® Cruciate Retaining (CR) Knee Replacement System TCR111111102

  Conformis, Inc. · Knee Arthroplasty Implantation System
  390 reports
• iTotal® Cruciate Retaining (CR) Knee Replacement System TCR111SPEC02

  Conformis, Inc. · Knee Arthroplasty Implantation System
  11 reports
• iTotal® Cruciate Retaining (CR) Knee Replacement System TCR121SPEC02

  Conformis, Inc. · Knee Arthroplasty Implantation System
  11 reports
• TRUMATCH 42-0906

  Depuy (Ireland) · Knee arthroplasty implantation system
  5 reports
• iTotal® Identity Cruciate Retaining Knee Replacement System TCR301111301

  Conformis, Inc. · Knee Arthroplasty Implantation System
  3 reports
• ITOTAL IDENTITY IMPACTOR ADAPTER 1080-213

  Conformis, Inc. · Knee Arthroplasty Implantation System
  1 report
• iTotal Identity 3DP Porous Knee TCR-000-D005-020111

  Restor3d, Inc. · Knee Arthroplasty Implantation System
  1 report
• VISIONAIRE V0200128

  Smith & Nephew, Inc. · Knee arthroplasty implantation system
  1 report
• My Knee Tibial Cutting Blocks 4.1032

  Medacta International SA · Knee Arthroplasty Implantation System
  1 report
• TRUMATCH 420902

  Depuy Orthopaedics, Inc. · Knee arthroplasty implantation system
  1 report
• TRUMATCH 420903

  Depuy Orthopaedics, Inc. · Knee arthroplasty implantation system
  1 report
• iTotal® CR iPoly™ Insert Kit RCR010000B03

  Conformis, Inc. · Knee Arthroplasty Implantation System
  1 report
• iTotal® CR iPoly™ Insert Kit RCR010080003

  Conformis, Inc. · Knee Arthroplasty Implantation System
  1 report
• iTotal Identity CR RCR301111301

  Conformis, Inc. · Knee Arthroplasty Implantation System
  1 report