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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 - 00887517886279

CoRoent Ant TLIF PEEK, 10x12x34mm 4°
Nuvasive, Inc.
5102344P2
In Commercial Distribution

  • 00887517886279 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517886262

CoRoent Ant TLIF PEEK, 10x12x34mm 12°
Nuvasive, Inc.
5102342P2
In Commercial Distribution

  • 00887517886262 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517886255

CoRoent Ant TLIF PEEK, 10x12x34mm 0°
Nuvasive, Inc.
5102340P2
In Commercial Distribution

  • 00887517886255 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517886248

CoRoent Ant TLIF PEEK, 10x12x32mm 8°
Nuvasive, Inc.
5102328P2
In Commercial Distribution

  • 00887517886248 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517886231

CoRoent Ant TLIF PEEK, 10x12x32mm 15°
Nuvasive, Inc.
5102325P2
In Commercial Distribution

  • 00887517886231 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517886224

CoRoent Ant TLIF PEEK, 10x12x32mm 4°
Nuvasive, Inc.
5102324P2
In Commercial Distribution

  • 00887517886224 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517886217

CoRoent Ant TLIF PEEK, 10x12x32mm 12°
Nuvasive, Inc.
5102322P2
In Commercial Distribution

  • 00887517886217 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517886200

CoRoent Ant TLIF PEEK, 10x12x32mm 0°
Nuvasive, Inc.
5102320P2
In Commercial Distribution

  • 00887517886200 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517886194

CoRoent Ant TLIF PEEK, 10x12x30mm 8°
Nuvasive, Inc.
5102308P2
In Commercial Distribution

  • 00887517886194 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517886187

CoRoent Ant TLIF PEEK, 10x12x30mm 15°
Nuvasive, Inc.
5102305P2
In Commercial Distribution

  • 00887517886187 ()


  • Metallic spinal interbody fusion cage
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