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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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XLX - 00887517940230

XLX ACR Interbody, 8x23x60mm
Nuvasive, Inc.
1675088
In Commercial Distribution

  • 00887517940230 ()


  • Metallic spinal interbody fusion cage

XLX - 00887517940223

XLX ACR Interbody, 6x23x60mm
Nuvasive, Inc.
1675087
In Commercial Distribution

  • 00887517940223 ()


  • Metallic spinal interbody fusion cage

XLX - 00887517940216

XLX ACR Interbody, 4x23x60mm
Nuvasive, Inc.
1675086
In Commercial Distribution

  • 00887517940216 ()


  • Metallic spinal interbody fusion cage

XLX - 00887517940209

XLX ACR Interbody, 12x23x55mm
Nuvasive, Inc.
1675085
In Commercial Distribution

  • 00887517940209 ()


  • Metallic spinal interbody fusion cage

XLX - 00887517940193

XLX ACR Interbody, 10x23x55mm
Nuvasive, Inc.
1675084
In Commercial Distribution

  • 00887517940193 ()


  • Metallic spinal interbody fusion cage

XLX - 00887517940186

XLX ACR Interbody, 8x23x55mm
Nuvasive, Inc.
1675083
In Commercial Distribution

  • 00887517940186 ()


  • Metallic spinal interbody fusion cage

XLX - 00887517940179

XLX ACR Interbody, 6x23x55mm
Nuvasive, Inc.
1675082
In Commercial Distribution

  • 00887517940179 ()


  • Metallic spinal interbody fusion cage

XLX - 00887517940162

XLX ACR Interbody, 4x23x55mm
Nuvasive, Inc.
1675081
In Commercial Distribution

  • 00887517940162 ()


  • Metallic spinal interbody fusion cage

XLX - 00887517940155

XLX ACR Interbody, 12x23x50mm
Nuvasive, Inc.
1675080
In Commercial Distribution

  • 00887517940155 ()


  • Metallic spinal interbody fusion cage

XLX - 00887517940148

XLX ACR Interbody, 10x23x50mm
Nuvasive, Inc.
1675079
In Commercial Distribution

  • 00887517940148 ()


  • Metallic spinal interbody fusion cage
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