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+, 7x22x50mm
Nuvasive, Inc.
6507250P2
In Commercial Distribution

  • 00887517993496 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W+, 7x22x45mm
Nuvasive, Inc.
6507245P2
In Commercial Distribution

  • 00887517993489 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W+, 6x22x60mm
Nuvasive, Inc.
6506260P2
In Commercial Distribution

  • 00887517993472 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W+, 6x22x55mm
Nuvasive, Inc.
6506255P2
In Commercial Distribution

  • 00887517993465 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W+, 6x22x50mm
Nuvasive, Inc.
6506250P2
In Commercial Distribution

  • 00887517993458 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W+, 6x22x45mm
Nuvasive, Inc.
6506245P2
In Commercial Distribution

  • 00887517993441 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 12x18x60mm 10°
Nuvasive, Inc.
6312860P2
In Commercial Distribution

  • 00887517993434 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 12x18x55mm 10°
Nuvasive, Inc.
6312855P2
In Commercial Distribution

  • 00887517993427 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 12x18x50mm 10°
Nuvasive, Inc.
6312850P2
In Commercial Distribution

  • 00887517993410 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 12x18x45mm 10°
Nuvasive, Inc.
6312845P2
In Commercial Distribution

  • 00887517993403 ()


  • Polymeric spinal fusion cage, sterile
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