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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Modulus TLIF-A, 10x9x30mm 15°
Nuvasive, Inc.
1109305P2
In Commercial Distribution

  • 00887517855275 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 10x14x40mm 8°
Nuvasive, Inc.
1104408P2
In Commercial Distribution

  • 00887517855091 ()


  • Polymeric spinal fusion cage, sterile
Modulus TLIF-A, 10x14x40mm 15°
Nuvasive, Inc.
1104405P2
In Commercial Distribution

  • 00887517855077 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 10x14x34mm 8°
Nuvasive, Inc.
1104348P2
In Commercial Distribution

  • 00887517854896 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 10x14x34mm 15°
Nuvasive, Inc.
1104345P2
In Commercial Distribution

  • 00887517854872 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 10x14x30mm 8°
Nuvasive, Inc.
1104308P2
In Commercial Distribution

  • 00887517854698 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 10x11x40mm 8°
Nuvasive, Inc.
1101408P2
In Commercial Distribution

  • 00887517853295 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 10x11x34mm 8°
Nuvasive, Inc.
1101348P2
In Commercial Distribution

  • 00887517853097 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 10x11x34mm 15°
Nuvasive, Inc.
1101345P2
In Commercial Distribution

  • 00887517853073 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-A, 10x11x30mm 8°
Nuvasive, Inc.
1101308P2
In Commercial Distribution

  • 00887517852892 ()


  • Metallic spinal interbody fusion cage
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