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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COHERE XLW, 12x22x50mm 15°
Nuvasive, Inc.
8151250P2
In Commercial Distribution

  • 00887517982346 ()


  • Polymeric spinal fusion cage, sterile
COHERE XLW, 12x22x45mm 15°
Nuvasive, Inc.
8151245P2
In Commercial Distribution

  • 00887517982322 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x60mm 15°
Nuvasive, Inc.
8151060P2
In Commercial Distribution

  • 00887517982308 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x55mm 15°
Nuvasive, Inc.
8151055P2
In Commercial Distribution

  • 00887517982285 ()


  • Polymeric spinal fusion cage, sterile
COHERE XLW, 10x22x50mm 15°
Nuvasive, Inc.
8151050P2
In Commercial Distribution

  • 00887517982261 ()


  • Polymeric spinal fusion cage, sterile
COHERE XLW, 10x22x45mm 15°
Nuvasive, Inc.
8151045P2
In Commercial Distribution

  • 00887517982247 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 8x22x60mm 15°
Nuvasive, Inc.
8150860P2
In Commercial Distribution

  • 00887517982223 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 8x22x55mm 15°
Nuvasive, Inc.
8150855P2
In Commercial Distribution

  • 00887517982209 ()


  • Polymeric spinal fusion cage, sterile
COHERE XLW, 8x22x50mm 15°
Nuvasive, Inc.
8150850P2
In Commercial Distribution

  • 00887517982186 ()


  • Polymeric spinal fusion cage, sterile
COHERE XLW, 8x22x45mm 15°
Nuvasive, Inc.
8150845P2
In Commercial Distribution

  • 00887517982162 ()


  • Polymeric spinal interbody fusion cage
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