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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Oblique TLIF, 14x10x30mm 8°
Nuvasive, Inc.
5340308P2
In Commercial Distribution

  • 00887517734952 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x30mm 4°
Nuvasive, Inc.
5340304P2
In Commercial Distribution

  • 00887517734945 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x30mm 12°
Nuvasive, Inc.
5340302P2
In Commercial Distribution

  • 00887517734938 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x30mm 0°
Nuvasive, Inc.
5340300P2
In Commercial Distribution

  • 00887517734921 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x25mm 8°
Nuvasive, Inc.
5340258P2
In Commercial Distribution

  • 00887517734914 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x25mm 4°
Nuvasive, Inc.
5340254P2
In Commercial Distribution

  • 00887517734907 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x25mm 12°
Nuvasive, Inc.
5340252P2
In Commercial Distribution

  • 00887517734891 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x30mm 4°
Nuvasive, Inc.
5334304P2
In Commercial Distribution

  • 00887517734785 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x30mm 12°
Nuvasive, Inc.
5334302P2
In Commercial Distribution

  • 00887517734778 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x30mm 0°
Nuvasive, Inc.
5334300P2
In Commercial Distribution

  • 00887517734761 ()


  • Polymeric spinal interbody fusion cage
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