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, 13x14x35mm 12°
Nuvasive, Inc.
5334352P2
In Commercial Distribution

  • 00887517734815 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x35mm 0°
Nuvasive, Inc.
5334350P2
In Commercial Distribution

  • 00887517734808 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x30mm 8°
Nuvasive, Inc.
5334308P2
In Commercial Distribution

  • 00887517734792 ()


  • 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
Oblique TLIF, 13x14x25mm 8°
Nuvasive, Inc.
5334258P2
In Commercial Distribution

  • 00887517734754 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x25mm 4°
Nuvasive, Inc.
5334254P2
In Commercial Distribution

  • 00887517734747 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x25mm 12°
Nuvasive, Inc.
5334252P2
In Commercial Distribution

  • 00887517734730 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x14x25mm 0°
Nuvasive, Inc.
5334250P2
In Commercial Distribution

  • 00887517734723 ()


  • Polymeric spinal interbody fusion cage
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