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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 Class Implantable

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CoRoent - 00887517897725

CoRoent Ant TLIF PEEK, 9x10x32mm 4°
Nuvasive, Inc.
5190324P2
In Commercial Distribution

  • 00887517897725 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517897718

CoRoent Ant TLIF PEEK, 9x10x32mm 12°
Nuvasive, Inc.
5190322P2
In Commercial Distribution

  • 00887517897718 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517897701

CoRoent Ant TLIF PEEK, 9x10x32mm 0°
Nuvasive, Inc.
5190320P2
In Commercial Distribution

  • 00887517897701 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517897695

CoRoent Ant TLIF PEEK, 9x10x30mm 8°
Nuvasive, Inc.
5190308P2
In Commercial Distribution

  • 00887517897695 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517897688

CoRoent Ant TLIF PEEK, 9x10x30mm 15°
Nuvasive, Inc.
5190305P2
In Commercial Distribution

  • 00887517897688 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517897671

CoRoent Ant TLIF PEEK, 9x10x30mm 4°
Nuvasive, Inc.
5190304P2
In Commercial Distribution

  • 00887517897671 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517897664

CoRoent Ant TLIF PEEK, 9x10x30mm 12°
Nuvasive, Inc.
5190302P2
In Commercial Distribution

  • 00887517897664 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517897657

CoRoent Ant TLIF PEEK, 9x10x30mm 0°
Nuvasive, Inc.
5190300P2
In Commercial Distribution

  • 00887517897657 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517897640

CoRoent Ant TLIF PEEK, 9x10x28mm 8°
Nuvasive, Inc.
5190288P2
In Commercial Distribution

  • 00887517897640 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517897633

CoRoent Ant TLIF PEEK, 9x10x28mm 15°
Nuvasive, Inc.
5190285P2
In Commercial Distribution

  • 00887517897633 ()


  • Metallic spinal interbody fusion cage
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