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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GENESIS II OXINIUM POSTERIOR STABILIZED FEMORAL RIGHT SIZE 2
Smith & Nephew, Inc.
71421112
In Commercial Distribution

  • 03596010469267 ()
71421112

  • Unicondylar knee prosthesis
GENESIS II OXINIUM P/S FEMORAL LT SZ 8
Smith & Nephew, Inc.
71421018
In Commercial Distribution

  • 03596010469243 ()
71421018

  • Unicondylar knee prosthesis
GENESIS II OXINIUM POSTERIOR STABILIZED FEMORAL LEFT SIZE 7
Smith & Nephew, Inc.
71421017
In Commercial Distribution

  • 03596010469236 ()
71421017

  • Unicondylar knee prosthesis
GENESIS II OXINIUM POSTERIOR STABILIZED FEMORAL LEFT SIZE 6
Smith & Nephew, Inc.
71421016
In Commercial Distribution

  • 03596010469229 ()
71421016

  • Unicondylar knee prosthesis
GENESIS II OXINIUM POSTERIOR STABILIZED FEMORAL LEFT SIZE 5
Smith & Nephew, Inc.
71421015
In Commercial Distribution

  • 03596010469212 ()
71421015

  • Unicondylar knee prosthesis
GENESIS II OXINIUM P/S FEMORAL LT SZ 4
Smith & Nephew, Inc.
71421014
In Commercial Distribution

  • 03596010469205 ()
71421014

  • Unicondylar knee prosthesis
GENESIS II OXINIUM P/S FEMORAL LT SZ 3
Smith & Nephew, Inc.
71421013
In Commercial Distribution

  • 03596010469199 ()
71421013

  • Unicondylar knee prosthesis
GENESIS II OXINIUM POSTERIOR STABILIZED FEMORAL LEFT SIZE 2
Smith & Nephew, Inc.
71421012
In Commercial Distribution

  • 03596010469182 ()
71421012

  • Unicondylar knee prosthesis
Partial Femoral Component, Full Post, Size Small-Medium, Right Medial
MAXX ORTHOPEDICS, INC.
314471
In Commercial Distribution

  • 00811767027762 ()


  • Unicondylar knee prosthesis
Partial Femoral Component, Full Post, Size XSmall, Right Medial
MAXX ORTHOPEDICS, INC.
314421
In Commercial Distribution

  • 00811767027755 ()


  • Unicondylar knee prosthesis
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