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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Tibial Plateau Plate STD 5mm
ONKOS SURGICAL, INC.
mktp/Std5
In Commercial Distribution


  • 5 millimeter
  • Standard
MKTP-STD5

  • Knee arthroplasty wedge
Tibial Plateau Plate STD 20mm
ONKOS SURGICAL, INC.
mktp/Std20
In Commercial Distribution


  • 20 millimeter
  • Standard
MKTP-STD20

  • Knee arthroplasty wedge
Tibial Plateau Plate STD 15mm
ONKOS SURGICAL, INC.
mktp/Std15
In Commercial Distribution


  • Standard
  • 15 millimeters
MKTP-STD15

  • Knee arthroplasty wedge
Tibial Plateau Plate STD 10mm
ONKOS SURGICAL, INC.
mktp/Std10
In Commercial Distribution


  • Standard
  • 10 millimeter
MKTP-STD10

  • Knee arthroplasty wedge
Tibial Plateau Plate SM 5mm
ONKOS SURGICAL, INC.
mktp/Sm5
In Commercial Distribution


  • 5 millimeter
  • Small
MKTP-SM5

  • Knee arthroplasty wedge
Tibial Plateau Plate SM 20mm
ONKOS SURGICAL, INC.
mktp/Sm20
In Commercial Distribution


  • 20 millimeters
  • Small
MKTP-SM20

  • Knee arthroplasty wedge
Tibial Plateau Plate SM 15mm
ONKOS SURGICAL, INC.
mktp/Sm15
In Commercial Distribution


  • 15 millimeters
  • Small
MKTP-SM15

  • Knee arthroplasty wedge
Tibial Plateau Plate SM 10mm
ONKOS SURGICAL, INC.
mktp/Sm10
In Commercial Distribution


  • 10 millimeter
  • Small
MKTP-SM10

  • Knee arthroplasty wedge
ADVANTIM® FEMORAL AUGMENT MD/MD+ LT/MEDIAL RT/LATERAL
Microport Orthopedics Inc.
18722114
In Commercial Distribution

  • 18722114 ()
  • M684187221141 ()
18722114

  • Knee arthroplasty wedge
ADVANTIM® FEMORAL AUGMENT MD/MD+ LT/LATERAL RT/MEDIAL
Microport Orthopedics Inc.
18722110
In Commercial Distribution

  • 18722110 ()
  • M684187221101 ()
18722110

  • Knee arthroplasty wedge
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