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 Class Implantable

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CoRoent XL-W, 10x22x60mm
Nuvasive, Inc.
6910260P
In Commercial Distribution

  • 00887517221360 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W, 12x22x55mm
Nuvasive, Inc.
6912255P
In Commercial Distribution

  • 00887517221322 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W, 8x22x55mm
Nuvasive, Inc.
6908255P
In Commercial Distribution

  • 00887517221308 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W, 14x22x50mm
Nuvasive, Inc.
6914250P
In Commercial Distribution

  • 00887517221087 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W, 10x22x50mm
Nuvasive, Inc.
6910250P
In Commercial Distribution

  • 00887517221063 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL, 14x18x60mm 10°
Nuvasive, Inc.
6981460P
In Commercial Distribution

  • 00887517220684 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL, 10x18x60mm 10°
Nuvasive, Inc.
6981060P
In Commercial Distribution

  • 00887517220660 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL, 16x18x55mm 10°
Nuvasive, Inc.
6981655P
In Commercial Distribution

  • 00887517220646 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL, 16x18x50mm 10°
Nuvasive, Inc.
6981650P
In Commercial Distribution

  • 00887517220295 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL, 12x18x50mm 10°
Nuvasive, Inc.
6981250P
In Commercial Distribution

  • 00887517220271 ()


  • Polymeric spinal fusion cage, sterile
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