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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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Brigade - 00887517419828

Brigade Hyperlordotic, 8x38x32mm 20°
Nuvasive, Inc.
7502120
In Commercial Distribution

  • 00887517419828 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517419811

Brigade Hyperlordotic, 6x38x32mm 20°
Nuvasive, Inc.
7502118
In Commercial Distribution

  • 00887517419811 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517419804

Brigade Hyperlordotic, 14x38x30mm 20°
Nuvasive, Inc.
7502117
In Commercial Distribution

  • 00887517419804 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517419491

Brigade Hyperlordotic, 12x38x30mm 20°
Nuvasive, Inc.
7502115
In Commercial Distribution

  • 00887517419491 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517419484

Brigade Hyperlordotic, 10x38x30mm 20°
Nuvasive, Inc.
7502113
In Commercial Distribution

  • 00887517419484 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517419439

Brigade Hyperlordotic, 10x38x28mm 20°
Nuvasive, Inc.
7502104
In Commercial Distribution

  • 00887517419439 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517681065

CoRoent XL-H, 10x22x60mm 20°
Nuvasive, Inc.
6201060P2
In Commercial Distribution

  • 00887517681065 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517681027

CoRoent XL-H, 10x22x40mm 20°
Nuvasive, Inc.
6201040P2
In Commercial Distribution

  • 00887517681027 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517681010

CoRoent XL-H, 8x22x60mm 20°
Nuvasive, Inc.
6200860P2
In Commercial Distribution

  • 00887517681010 ()


  • Polymeric spinal interbody fusion cage

Halyard - 30680651793561

HYH,OPTH,DRAPE,-,-,20
O&M HALYARD, INC.
79356
In Commercial Distribution

  • 30680651793561 ()
  • 90680651793563 ()


  • Patient surgical drape, single-use, non-sterile
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