SEARCH RESULTS FOR: Femoral(38905 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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Femoral distal augment trial, #5, 8mm
UNITED ORTHOPEDIC CORP.
2623-6352
In Commercial Distribution

  • 04719886907629 ()
2623-6352

  • Knee femur prosthesis trial, reusable
Femoral distal augment trial, #5, 4mm
UNITED ORTHOPEDIC CORP.
2623-6351
In Commercial Distribution

  • 04719886907612 ()
2623-6351

  • Knee femur prosthesis trial, reusable
Femoral distal augment trial, #4, 8mm
UNITED ORTHOPEDIC CORP.
2623-6342
In Commercial Distribution

  • 04719886907582 ()
2623-6342

  • Knee femur prosthesis trial, reusable
Femoral distal augment trial, #4, 4mm
UNITED ORTHOPEDIC CORP.
2623-6341
In Commercial Distribution

  • 04719886907575 ()
2623-6341

  • Knee femur prosthesis trial, reusable
Femoral posterior augment trial, #6, 8mm
UNITED ORTHOPEDIC CORP.
2623-6062
In Commercial Distribution

  • 04719886907322 ()
2623-6062

  • Knee femur prosthesis trial, reusable
Femoral posterior augment trial, #5, 8mm
UNITED ORTHOPEDIC CORP.
2623-6052
In Commercial Distribution

  • 04719886907315 ()
2623-6052

  • Knee femur prosthesis trial, reusable
Femoral posterior augment trial, #4, 8mm
UNITED ORTHOPEDIC CORP.
2623-6042
In Commercial Distribution

  • 04719886907308 ()
2623-6042

  • Knee femur prosthesis trial, reusable
Femoral posterior augment trial, #3, 8mm
UNITED ORTHOPEDIC CORP.
2623-6032
In Commercial Distribution

  • 04719886907292 ()
2623-6032

  • Knee femur prosthesis trial, reusable
Femoral posterior augment trial, #2, 8mm
UNITED ORTHOPEDIC CORP.
2623-6022
In Commercial Distribution

  • 04719886907285 ()
2623-6022

  • Knee femur prosthesis trial, reusable
Femoral posterior augment trial, #1, 8mm
UNITED ORTHOPEDIC CORP.
2623-6012
In Commercial Distribution

  • 04719886907278 ()
2623-6012

  • Knee femur prosthesis trial, reusable
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