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 XLW Ti, 14x22x55mm 10°
Nuvasive, Inc.
6421455
In Commercial Distribution

  • 00887517311382 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 14x22x50mm 10°
Nuvasive, Inc.
6421450
In Commercial Distribution

  • 00887517311375 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 14x22x45mm 10°
Nuvasive, Inc.
6421445
In Commercial Distribution

  • 00887517311368 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 14x22x40mm 10°
Nuvasive, Inc.
6421440
In Commercial Distribution

  • 00887517311351 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 12x22x60mm 10°
Nuvasive, Inc.
6421260
In Commercial Distribution

  • 00887517311344 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 12x22x55mm 10°
Nuvasive, Inc.
6421255
In Commercial Distribution

  • 00887517311337 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 12x22x50mm 10°
Nuvasive, Inc.
6421250
In Commercial Distribution

  • 00887517311320 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 12x22x45mm 10°
Nuvasive, Inc.
6421245
In Commercial Distribution

  • 00887517311313 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 12x22x40mm 10°
Nuvasive, Inc.
6421240
In Commercial Distribution

  • 00887517311306 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 10x22x60mm 10°
Nuvasive, Inc.
6421060
In Commercial Distribution

  • 00887517310996 ()


  • Polymeric spinal interbody fusion cage
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