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® XL-W+, 10x22x50mm
Nuvasive, Inc.
6510250
In Commercial Distribution

  • 00887517313669 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 10x22x45mm
Nuvasive, Inc.
6510245
In Commercial Distribution

  • 00887517313652 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 10x22x40mm
Nuvasive, Inc.
6510240
In Commercial Distribution

  • 00887517313645 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 8x22x60mm
Nuvasive, Inc.
6508260
In Commercial Distribution

  • 00887517313263 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 8x22x55mm
Nuvasive, Inc.
6508255
In Commercial Distribution

  • 00887517313256 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 8x22x50mm
Nuvasive, Inc.
6508250
In Commercial Distribution

  • 00887517313249 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 8x22x45mm
Nuvasive, Inc.
6508245
In Commercial Distribution

  • 00887517313232 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 8x22x40mm
Nuvasive, Inc.
6508240
In Commercial Distribution

  • 00887517313225 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 6x22x40mm
Nuvasive, Inc.
6506240
In Commercial Distribution

  • 00887517312808 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 16x18x60mm 10°
Nuvasive, Inc.
6481660
In Commercial Distribution

  • 00887517312495 ()


  • Polymeric spinal interbody fusion cage
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