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® XLW Ti, 12x22x40mm
Nuvasive, Inc.
6412240
In Commercial Distribution

  • 00887517310156 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 10x22x60mm
Nuvasive, Inc.
6410260
In Commercial Distribution

  • 00887517310149 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 10x22x55mm
Nuvasive, Inc.
6410255
In Commercial Distribution

  • 00887517310132 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 10x22x50mm
Nuvasive, Inc.
6410250
In Commercial Distribution

  • 00887517310125 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 10x22x45mm
Nuvasive, Inc.
6410245
In Commercial Distribution

  • 00887517310118 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 10x18x55mm 10°
Nuvasive, Inc.
6310855
In Commercial Distribution

  • 00887517306579 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 10x18x50mm 10°
Nuvasive, Inc.
6310850
In Commercial Distribution

  • 00887517306562 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 10x18x45mm 10°
Nuvasive, Inc.
6310845
In Commercial Distribution

  • 00887517306555 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 10x18x40mm 10°
Nuvasive, Inc.
6310840
In Commercial Distribution

  • 00887517306548 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 10x22x60mm 10°
Nuvasive, Inc.
6310260
In Commercial Distribution

  • 00887517306524 ()


  • Polymeric spinal interbody fusion cage
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