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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 Size Type Device Class Implantable

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Posterior Interbody Fusion Device PEEK/Ti 9x25x10 L5°
Medacta International SA
03.27.138
In Commercial Distribution

  • 07630040719681 ()


  • Metallic spinal interbody fusion cage
Posterior Interbody Fusion Device PEEK/Ti 9x25x9 L5°
Medacta International SA
03.27.137
In Commercial Distribution

  • 07630040719674 ()


  • Metallic spinal interbody fusion cage
Posterior Interbody Fusion Device PEEK/Ti 9x25x8 L5°
Medacta International SA
03.27.136
In Commercial Distribution

  • 07630040719667 ()


  • Metallic spinal interbody fusion cage
Posterior Interbody Fusion Device PEEK/Ti 9x25x7 L5°
Medacta International SA
03.27.135
In Commercial Distribution

  • 07630040719650 ()


  • Metallic spinal interbody fusion cage
Posterior Interbody Fusion Device PEEK/Ti 9x25x15 L0°
Medacta International SA
03.27.134
In Commercial Distribution

  • 07630040719643 ()


  • Metallic spinal interbody fusion cage
Posterior Interbody Fusion Device PEEK/Ti 9x25x14 L0°
Medacta International SA
03.27.133
In Commercial Distribution

  • 07630040719636 ()


  • Metallic spinal interbody fusion cage
Posterior Interbody Fusion Device PEEK/Ti 9x25x13 L0°
Medacta International SA
03.27.132
In Commercial Distribution

  • 07630040719629 ()


  • Metallic spinal interbody fusion cage
Posterior Interbody Fusion Device PEEK/Ti 9x25x12 L0°
Medacta International SA
03.27.131
In Commercial Distribution

  • 07630040719612 ()


  • Metallic spinal interbody fusion cage
Posterior Interbody Fusion Device PEEK/Ti 9x25x11 L0°
Medacta International SA
03.27.130
In Commercial Distribution

  • 07630040719605 ()


  • Metallic spinal interbody fusion cage
Posterior Interbody Fusion Device PEEK/Ti 9x25x10 L0°
Medacta International SA
03.27.129
In Commercial Distribution

  • 07630040719599 ()


  • Metallic spinal interbody fusion cage
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