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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 Class Implantable

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CoRoent Sm ACR Ta Marker, 12x19x16mm 15°
Nuvasive, Inc.
6733312
In Commercial Distribution

  • 00887517531629 ()


  • Polymeric spinal interbody fusion cage
CoRoent Sm ACR Ta Marker, 11x19x16mm 15°
Nuvasive, Inc.
6733311
In Commercial Distribution

  • 00887517531612 ()


  • Polymeric spinal interbody fusion cage
CoRoent Sm ACR Ta Marker, 10x19x16mm 15°
Nuvasive, Inc.
6733310
In Commercial Distribution

  • 00887517531605 ()


  • Polymeric spinal interbody fusion cage
CoRoent Sm ACR Ta Marker, 9x19x16mm 15°
Nuvasive, Inc.
6733309
In Commercial Distribution

  • 00887517531599 ()


  • Polymeric spinal interbody fusion cage
CoRoent Sm ACR Ta Marker, 8x19x16mm 15°
Nuvasive, Inc.
6733308
In Commercial Distribution

  • 00887517531582 ()


  • Polymeric spinal interbody fusion cage
CoRoent Sm ACR Ta Marker, 7x19x16mm 15°
Nuvasive, Inc.
6733307
In Commercial Distribution

  • 00887517531575 ()


  • Polymeric spinal interbody fusion cage
CoRoent Sm ACR Ta Marker, 12x19x16mm 10°
Nuvasive, Inc.
6733212
In Commercial Distribution

  • 00887517531520 ()


  • Polymeric spinal interbody fusion cage
CoRoent Sm ACR Ta Marker, 11x19x16mm 10°
Nuvasive, Inc.
6733211
In Commercial Distribution

  • 00887517531513 ()


  • Polymeric spinal interbody fusion cage
CoRoent Sm ACR Ta Marker, 10x19x16mm 10°
Nuvasive, Inc.
6733210
In Commercial Distribution

  • 00887517531506 ()


  • Polymeric spinal interbody fusion cage
CoRoent Sm ACR Ta Marker, 9x19x16mm 10°
Nuvasive, Inc.
6733209
In Commercial Distribution

  • 00887517531490 ()


  • Polymeric spinal interbody fusion cage
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