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
GENESIS II DISTAL FEMORAL WEDGE TRIAL SIZE 8 5MM
Smith & Nephew, Inc.
71430671
In Commercial Distribution

  • 03596010212733 ()
71430671

  • 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 5 5MM
Smith & Nephew, Inc.
71430668
In Commercial Distribution

  • 03596010212702 ()
71430668

  • 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 3 5MM
Smith & Nephew, Inc.
71430666
In Commercial Distribution

  • 03596010212689 ()
71430666

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

  • 03596010212672 ()
71430665

  • Knee arthroplasty wedge
GENESIS II DISTAL FEMORAL WEDGE TRIAL SIZE 1 5MM
Smith & Nephew, Inc.
71430664
In Commercial Distribution

  • 03596010212665 ()
71430664

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE 7-8 5MM SHORT
Smith & Nephew, Inc.
71420692
Not in Commercial Distribution

  • 03596010208958 ()
71420692

  • Knee arthroplasty wedge
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