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, 12x14x30mm 12°
Nuvasive, Inc.
5324302P2
In Commercial Distribution

  • 00887517734433 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x14x25mm 0°
Nuvasive, Inc.
5324250P2
In Commercial Distribution

  • 00887517734389 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x10x25mm 15°
Nuvasive, Inc.
5322515P2
In Commercial Distribution

  • 00887517734365 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x10x40mm 8°
Nuvasive, Inc.
5320408P2
In Commercial Distribution

  • 00887517734358 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x10x40mm 12°
Nuvasive, Inc.
5320402P2
In Commercial Distribution

  • 00887517734334 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x10x35mm 8°
Nuvasive, Inc.
5320358P2
In Commercial Distribution

  • 00887517734310 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x10x35mm 4°
Nuvasive, Inc.
5320354P2
In Commercial Distribution

  • 00887517734303 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x10x35mm 12°
Nuvasive, Inc.
5320352P2
In Commercial Distribution

  • 00887517734297 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x10x35mm 0°
Nuvasive, Inc.
5320350P2
In Commercial Distribution

  • 00887517734280 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 12x10x30mm 8°
Nuvasive, Inc.
5320308P2
In Commercial Distribution

  • 00887517734273 ()


  • Polymeric spinal interbody fusion cage
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