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, 8x10x35mm 4°
Nuvasive, Inc.
5380354P2
In Commercial Distribution

  • 00887517736468 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x35mm 12°
Nuvasive, Inc.
5380352P2
In Commercial Distribution

  • 00887517736451 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x35mm 0°
Nuvasive, Inc.
5380350P2
In Commercial Distribution

  • 00887517736444 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x30mm 8°
Nuvasive, Inc.
5380308P2
In Commercial Distribution

  • 00887517736437 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x30mm 4°
Nuvasive, Inc.
5380304P2
In Commercial Distribution

  • 00887517736420 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x30mm 12°
Nuvasive, Inc.
5380302P2
In Commercial Distribution

  • 00887517736413 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x30mm 0°
Nuvasive, Inc.
5380300P2
In Commercial Distribution

  • 00887517736406 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x25mm 8°
Nuvasive, Inc.
5380258P2
In Commercial Distribution

  • 00887517736390 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x25mm 4°
Nuvasive, Inc.
5380254P2
In Commercial Distribution

  • 00887517736383 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 8x10x25mm 12°
Nuvasive, Inc.
5380252P2
In Commercial Distribution

  • 00887517736376 ()


  • Polymeric spinal interbody fusion cage
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