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, 13x10x40mm 0°
Nuvasive, Inc.
5330400P2
In Commercial Distribution

  • 00887517734662 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x10x35mm 4°
Nuvasive, Inc.
5330354P2
In Commercial Distribution

  • 00887517734648 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x10x35mm 0°
Nuvasive, Inc.
5330350P2
In Commercial Distribution

  • 00887517734624 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x10x30mm 4°
Nuvasive, Inc.
5330304P2
In Commercial Distribution

  • 00887517734600 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x10x30mm 0°
Nuvasive, Inc.
5330300P2
In Commercial Distribution

  • 00887517734587 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 13x10x25mm 8°
Nuvasive, Inc.
5330258P2
In Commercial Distribution

  • 00887517734570 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x14x40mm 4°
Nuvasive, Inc.
5324404P2
In Commercial Distribution

  • 00887517734525 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x14x40mm 0°
Nuvasive, Inc.
5324400P2
In Commercial Distribution

  • 00887517734501 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x14x35mm 4°
Nuvasive, Inc.
5324354P2
In Commercial Distribution

  • 00887517734488 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x14x35mm 0°
Nuvasive, Inc.
5324350P2
In Commercial Distribution

  • 00887517734464 ()


  • Polymeric spinal interbody fusion cage
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