SEARCH RESULTS FOR: Femoral(2076 results)

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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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KNEE RT 66 - M209102400

No Description
BIOPRO, INC.
10240
In Commercial Distribution

  • M209102400 ()


  • Coated knee femur prosthesis

KNEE LT 86 - M209102220

No Description
BIOPRO, INC.
10222
In Commercial Distribution

  • M209102220 ()


  • Coated knee femur prosthesis

KNEE LT 82 - M209102210

No Description
BIOPRO, INC.
10221
In Commercial Distribution

  • M209102210 ()


  • Coated knee femur prosthesis

KNEE LT 74 - M209102190

No Description
BIOPRO, INC.
10219
In Commercial Distribution

  • M209102190 ()


  • Coated knee femur prosthesis

KNEE LT 70 - M209102180

No Description
BIOPRO, INC.
10218
In Commercial Distribution

  • M209102180 ()


  • Coated knee femur prosthesis

KNEE LT 62 - M209102160

No Description
BIOPRO, INC.
10216
In Commercial Distribution

  • M209102160 ()


  • Coated knee femur prosthesis

GENESIS II - 00885556056875

GENESIS II HYRDOXYAPATITE POROUS Posterior Stabilized FEMORALS SIZE 6 RIGHT
Smith & Nephew, Inc.
71931639
In Commercial Distribution

  • 00885556056875 ()
71931639

  • Coated knee femur prosthesis

GENESIS II - 00885556056769

GENESIS II HYRDOXYAPATITE POROUS Posterior Stabilized FEMORALS SIZE 5 LEFT
Smith & Nephew, Inc.
71931644
In Commercial Distribution

  • 00885556056769 ()
71931644

  • Coated knee femur prosthesis

GENESIS II - 00885556056431

GENESIS II HYRDOXYAPATITE POROUS Posterior Stabilized FEMORALS SIZE 4 LEFT
Smith & Nephew, Inc.
71931643
In Commercial Distribution

  • 00885556056431 ()
71931643

  • Coated knee femur prosthesis

GENESIS II - 00885556056356

GENESIS II HYRDOXYAPATITE POROUS Posterior Stabilized FEMORALS SIZE 5 RIGHT
Smith & Nephew, Inc.
71931638
In Commercial Distribution

  • 00885556056356 ()
71931638

  • Coated knee femur prosthesis
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