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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 Class Implantable

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APX - 00887517454041

XLIF APX, 10x26x55mm 10°
Nuvasive, Inc.
1672353
In Commercial Distribution

  • 00887517454041 ()


  • Metallic spinal interbody fusion cage

APX - 00887517454010

XLIF APX, 12x30x50mm 10°
Nuvasive, Inc.
1672383
In Commercial Distribution

  • 00887517454010 ()


  • Metallic spinal interbody fusion cage

APX - 00887517454003

XLIF APX, 12x26x50mm 10°
Nuvasive, Inc.
1672380
In Commercial Distribution

  • 00887517454003 ()


  • Metallic spinal interbody fusion cage

APX - 00887517453693

XLIF APX, 12x26x50mm 0°
Nuvasive, Inc.
1672379
In Commercial Distribution

  • 00887517453693 ()


  • Metallic spinal interbody fusion cage

APX - 00887517453686

XLIF APX, 10x30x50mm 10°
Nuvasive, Inc.
1672347
In Commercial Distribution

  • 00887517453686 ()


  • Metallic spinal interbody fusion cage

APX - 00887517451903

XLIF APX, 10x26x50mm 10°
Nuvasive, Inc.
1672344
In Commercial Distribution

  • 00887517451903 ()


  • Metallic spinal interbody fusion cage

APX - 00887517451590

XLIF APX, 10x26x50mm 0°
Nuvasive, Inc.
1672343
In Commercial Distribution

  • 00887517451590 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517362575

CoRoent® XL-XW ST, 10x26x65mm 10° Left
Nuvasive, Inc.
1618888
In Commercial Distribution

  • 00887517362575 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517361745

CoRoent® XL-XW ST, 12x26x60mm 10° Left
Nuvasive, Inc.
1618865
In Commercial Distribution

  • 00887517361745 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517361721

CoRoent® XL-XW ST, 10x26x60mm 10° Left
Nuvasive, Inc.
1618863
In Commercial Distribution

  • 00887517361721 ()


  • Polymeric spinal interbody fusion cage
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