SEARCH RESULTS FOR: Femoral(1408 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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TRAY UNI XLG - M209103230

No Description
BIOPRO, INC.
10323
In Commercial Distribution

  • M209103230 ()


  • Unicondylar knee prosthesis

TRAY UNI LG - M209103220

No Description
BIOPRO, INC.
10322
In Commercial Distribution

  • M209103220 ()


  • Unicondylar knee prosthesis

TRAY UNI MD - M209103210

No Description
BIOPRO, INC.
10321
In Commercial Distribution

  • M209103210 ()


  • Unicondylar knee prosthesis

TRAY UNI SM - M209103200

No Description
BIOPRO, INC.
10320
In Commercial Distribution

  • M209103200 ()


  • Unicondylar knee prosthesis

JOURNEY II - 00885556578834

JOURNEY II UNI TIBIAL BASEPLATE SIZE 6 RM/LL
Smith & Nephew, Inc.
71935204
In Commercial Distribution

  • 00885556578834 ()
71935204

  • Unicondylar knee prosthesis

JOURNEY II - 00885556578827

JOURNEY II UNI TIBIAL BASEPLATE SIZE 5 RM/LL
Smith & Nephew, Inc.
71935203
In Commercial Distribution

  • 00885556578827 ()
71935203

  • Unicondylar knee prosthesis

JOURNEY II - 00885556578810

JOURNEY II UNI TIBIAL BASEPLATE SIZE 4 RM/LL
Smith & Nephew, Inc.
71935202
In Commercial Distribution

  • 00885556578810 ()
71935202

  • Unicondylar knee prosthesis

JOURNEY II - 00885556578797

JOURNEY II UNI TIBIAL BASEPLATE SIZE 2 RM/LL
Smith & Nephew, Inc.
71935200
In Commercial Distribution

  • 00885556578797 ()
71935200

  • Unicondylar knee prosthesis

JOURNEY II - 00885556578780

JOURNEY II UNI TIBIAL BASEPLATE SIZE 1 RM/LL
Smith & Nephew, Inc.
71935199
In Commercial Distribution

  • 00885556578780 ()
71935199

  • Unicondylar knee prosthesis

JOURNEY II - 00885556578773

JOURNEY II UNI TIBIAL BASEPLATE SIZE 6 LM/RL
Smith & Nephew, Inc.
71935198
In Commercial Distribution

  • 00885556578773 ()
71935198

  • Unicondylar knee prosthesis
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