Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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LEGION SCREW-ON POSTERIOR FEMORAL WEDGE 5MM SIZE 1-2 LONG
Smith & Nephew, Inc.
71421801
In Commercial Distribution

  • 03596010545350 ()
71421801

  • Knee arthroplasty wedge
LEGION SCREW-ON POSTERIOR FEMORAL WEDGE 5MM SIZE 7-8 LONG
Smith & Nephew, Inc.
71421807
In Commercial Distribution

  • 03596010545411 ()
71421807

  • Knee arthroplasty wedge
LEGION SCREW-ON POSTERIOR FEMORAL WEDGE 5MM SIZE 5-6 LONG
Smith & Nephew, Inc.
71421805
In Commercial Distribution

  • 03596010545398 ()
71421805

  • Knee arthroplasty wedge
LEGION SCREW-ON POSTERIOR FEMORAL WEDGE 10MM SIZE 3-4 LONG
Smith & Nephew, Inc.
71421804
In Commercial Distribution

  • 03596010545381 ()
71421804

  • Knee arthroplasty wedge
LEGION SCREW-ON POSTERIOR FEMORAL WEDGE 5MM SIZE 3-4 LONG
Smith & Nephew, Inc.
71421803
In Commercial Distribution

  • 03596010545374 ()
71421803

  • Knee arthroplasty wedge
LEGION SCREW-ON POSTERIOR FEMORAL WEDGE 10MM SIZE 1-2 LONG
Smith & Nephew, Inc.
71421802
In Commercial Distribution

  • 03596010545367 ()
71421802

  • Knee arthroplasty wedge
GENESIS II DISTAL FEMORAL WEDGE TRIAL SIZE 7 5MM
Smith & Nephew, Inc.
71430670
In Commercial Distribution

  • 03596010212726 ()
71430670

  • Knee arthroplasty wedge
GENESIS II DISTAL FEMORAL WEDGE TRIAL SIZE 6 5MM
Smith & Nephew, Inc.
71430669
In Commercial Distribution

  • 03596010212719 ()
71430669

  • Knee arthroplasty wedge
GENESIS II DISTAL FEMORAL WEDGE TRIAL SIZE 4 5MM
Smith & Nephew, Inc.
71430667
In Commercial Distribution

  • 03596010212696 ()
71430667

  • Knee arthroplasty wedge
GENESIS II DISTAL FEMORAL WEDGE TRIAL SIZE 2 5MM
Smith & Nephew, Inc.
71430665
In Commercial Distribution

  • 03596010212672 ()
71430665

  • Knee arthroplasty wedge
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