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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CoRoent® XL Wide, 12x22x50mm Lordotic
Nuvasive, Inc.
6921250
In Commercial Distribution

  • 00887517394118 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 12x22x45mm Lordotic
Nuvasive, Inc.
6921245
In Commercial Distribution

  • 00887517394101 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLR, 12x34x24 8°
Nuvasive, Inc.
6921244
In Commercial Distribution

  • 00887517393791 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLR, 10x38x28 8°
Nuvasive, Inc.
6921088
In Commercial Distribution

  • 00887517393722 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 10x22x60mm Lordotic
Nuvasive, Inc.
6921060
In Commercial Distribution

  • 00887517393715 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 10x22x55mm Lordotic
Nuvasive, Inc.
6921055
In Commercial Distribution

  • 00887517393708 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 10x22x50mm Lordotic
Nuvasive, Inc.
6921050
In Commercial Distribution

  • 00887517393395 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 10x22x45mm Lordotic
Nuvasive, Inc.
6921045
In Commercial Distribution

  • 00887517393388 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLR, 10x34x24 8°
Nuvasive, Inc.
6921044
In Commercial Distribution

  • 00887517393371 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 8x22x60mm Lordotic
Nuvasive, Inc.
6920860
In Commercial Distribution

  • 00887517393333 ()


  • Polymeric spinal interbody fusion cage
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