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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JOURNEY II OUTLIER SIZE 10 KIT
Smith & Nephew, Inc.
74010100KT
In Commercial Distribution

  • 00885556291795 ()
74010100KT

  • Unicondylar knee prosthesis
JOURNEY II OUTLIER SIZE 9 KIT
Smith & Nephew, Inc.
74010099KT
In Commercial Distribution

  • 00885556291740 ()
74010099KT

  • Unicondylar knee prosthesis
JOURNEY II OUTLIER SIZE 2 KIT
Smith & Nephew, Inc.
74010098KT
In Commercial Distribution

  • 00885556291696 ()
74010098KT

  • Unicondylar knee prosthesis
JOURNEY II OUTLIER SIZE 1 KIT
Smith & Nephew, Inc.
74010097KT
In Commercial Distribution

  • 00885556291641 ()
74010097KT

  • Unicondylar knee prosthesis
LEGION NARROW Posterior Stabilized OXINIUM SIZE 6N RIGHT
Smith & Nephew, Inc.
71421276
In Commercial Distribution

  • 00885556234259 ()
71421276

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

  • 00885556578834 ()
71935204

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

  • 00885556578827 ()
71935203

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

  • 00885556578810 ()
71935202

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

  • 00885556578797 ()
71935200

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

  • 00885556578780 ()
71935199

  • Unicondylar knee prosthesis
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