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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Oblique TLIF, 11x10x40mm 12°
Nuvasive, Inc.
5310402P2
In Commercial Distribution

  • 00887517733993 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x10x35mm 8°
Nuvasive, Inc.
5310358P2
In Commercial Distribution

  • 00887517733979 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x10x30mm 12°
Nuvasive, Inc.
5310302P2
In Commercial Distribution

  • 00887517733917 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x10x25mm 8°
Nuvasive, Inc.
5310258P2
In Commercial Distribution

  • 00887517733894 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x10x25mm 12°
Nuvasive, Inc.
5310252P2
In Commercial Distribution

  • 00887517733870 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x40mm 8°
Nuvasive, Inc.
5304408P2
In Commercial Distribution

  • 00887517733856 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x40mm 12°
Nuvasive, Inc.
5304402P2
In Commercial Distribution

  • 00887517733832 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x35mm 8°
Nuvasive, Inc.
5304358P2
In Commercial Distribution

  • 00887517733818 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x35mm 12°
Nuvasive, Inc.
5304352P2
In Commercial Distribution

  • 00887517733795 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x30mm 8°
Nuvasive, Inc.
5304308P2
In Commercial Distribution

  • 00887517733771 ()


  • Polymeric spinal interbody fusion cage
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