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® XL-H, 10x22x45mm 30°
Nuvasive, Inc.
6301045
In Commercial Distribution

  • 00887517304353 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 8x22x60mm 30°
Nuvasive, Inc.
6300860
In Commercial Distribution

  • 00887517304322 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 8x22x55mm 30°
Nuvasive, Inc.
6300855
In Commercial Distribution

  • 00887517304315 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 8x22x50mm 30°
Nuvasive, Inc.
6300850
In Commercial Distribution

  • 00887517304308 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 8x22x45mm 30°
Nuvasive, Inc.
6300845
In Commercial Distribution

  • 00887517303998 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 6x22x60mm 30°
Nuvasive, Inc.
6300660
In Commercial Distribution

  • 00887517303967 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 6x22x55mm 30°
Nuvasive, Inc.
6300655
In Commercial Distribution

  • 00887517303950 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 6x22x50mm 30°
Nuvasive, Inc.
6300650
In Commercial Distribution

  • 00887517303943 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 6x22x45mm 30°
Nuvasive, Inc.
6300645
In Commercial Distribution

  • 00887517303936 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 4x22x60mm 30°
Nuvasive, Inc.
6300460
In Commercial Distribution

  • 00887517303905 ()


  • Polymeric spinal interbody fusion cage
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