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+, 10x18x55mm 10° Bulleted
Nuvasive, Inc.
1625461
In Commercial Distribution

  • 00887517229083 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 10x18x50mm 10° Bulleted
Nuvasive, Inc.
1625460
In Commercial Distribution

  • 00887517229076 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 10x18x45mm 10° Bulleted
Nuvasive, Inc.
1625459
In Commercial Distribution

  • 00887517229069 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 8x18x60mm 10° Bulleted
Nuvasive, Inc.
1625454
In Commercial Distribution

  • 00887517229014 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 8x18x55mm 10° Bulleted
Nuvasive, Inc.
1625453
In Commercial Distribution

  • 00887517229007 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 8x18x50mm 10° Bulleted
Nuvasive, Inc.
1625452
In Commercial Distribution

  • 00887517217745 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 8x18x45mm 10° Bulleted
Nuvasive, Inc.
1625451
In Commercial Distribution

  • 00887517217738 ()


  • Polymeric spinal interbody fusion cage
CoRoent LC, 16x11x30mm 8°
Nuvasive, Inc.
6616130
In Commercial Distribution

  • 00887517203465 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LC, 14x9x30mm 8°
Nuvasive, Inc.
6614930
In Commercial Distribution

  • 00887517203403 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LC, 14x11x30mm 8°
Nuvasive, Inc.
6614130
In Commercial Distribution

  • 00887517202987 ()


  • Polymeric spinal interbody fusion cage
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