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 Class Implantable

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CoRoent® XLCT, 12x18x60mm 10°
Nuvasive, Inc.
6111260
In Commercial Distribution

  • 00887517288073 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLCT, 12x18x50mm 10°
Nuvasive, Inc.
6111250
In Commercial Distribution

  • 00887517288059 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLCT, 10x18x55mm 10°
Nuvasive, Inc.
6111055
In Commercial Distribution

  • 00887517288004 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-CTW, 14x22x55mm, 10°
Nuvasive, Inc.
7221455
In Commercial Distribution

  • 00887517287892 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-CTW, 14x22x50mm, 10°
Nuvasive, Inc.
7221450
In Commercial Distribution

  • 00887517287885 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-CTW, 14x22x45mm, 10°
Nuvasive, Inc.
7221445
In Commercial Distribution

  • 00887517287878 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-CTW, 12x22x60mm, 10°
Nuvasive, Inc.
7221260
In Commercial Distribution

  • 00887517287809 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLCT, 10x18x45mm 10°
Nuvasive, Inc.
6111045
In Commercial Distribution

  • 00887517287687 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LC Ti, 10x11x30mm 8°
Nuvasive, Inc.
6110130
In Commercial Distribution

  • 00887517287656 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-CTW, 12x22x55mm, 10°
Nuvasive, Inc.
7221255
In Commercial Distribution

  • 00887517287496 ()


  • Polymeric spinal interbody fusion cage
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