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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COHERE XL, 12x18x55mm 0°
Nuvasive, Inc.
8187255P2
In Commercial Distribution

  • 00887517983008 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 12x18x50mm 0°
Nuvasive, Inc.
8187250P2
In Commercial Distribution

  • 00887517982988 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 12x18x45mm 0°
Nuvasive, Inc.
8187245P2
In Commercial Distribution

  • 00887517982964 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 10x18x60mm 0°
Nuvasive, Inc.
8187160P2
In Commercial Distribution

  • 00887517982940 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 10x18x55mm 0°
Nuvasive, Inc.
8187155P2
In Commercial Distribution

  • 00887517982926 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 10x18x50mm 0°
Nuvasive, Inc.
8187150P2
In Commercial Distribution

  • 00887517982902 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 10x18x45mm 0°
Nuvasive, Inc.
8187145P2
In Commercial Distribution

  • 00887517982889 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 12x18x60mm 10°
Nuvasive, Inc.
8181260P2
In Commercial Distribution

  • 00887517982865 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 12x18x55mm 10°
Nuvasive, Inc.
8181255P2
In Commercial Distribution

  • 00887517982841 ()


  • Polymeric spinal fusion cage, sterile
COHERE XL, 12x18x50mm 10°
Nuvasive, Inc.
8181250P2
In Commercial Distribution

  • 00887517982827 ()


  • Polymeric spinal fusion cage, sterile
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