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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 Size Type Device Class Implantable

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COHERE ALIF Interbody, 10x38x28mm 25°
Nuvasive, Inc.
1908825P2
In Commercial Distribution

  • 00195377067135 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x38x28mm 20°
Nuvasive, Inc.
1908820P2
In Commercial Distribution

  • 00195377067128 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x38x28mm 15°
Nuvasive, Inc.
1908815P2
In Commercial Distribution

  • 00195377067111 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x38x28mm 10°
Nuvasive, Inc.
1908810P2
In Commercial Distribution

  • 00195377067104 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x26x22mm 20°
Nuvasive, Inc.
1906220P2
In Commercial Distribution

  • 00195377067098 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x26x22mm 15°
Nuvasive, Inc.
1906215P2
In Commercial Distribution

  • 00195377067081 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x26x22mm 10°
Nuvasive, Inc.
1906210P2
In Commercial Distribution

  • 00195377067074 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x34x24mm 30°
Nuvasive, Inc.
1904430P2
In Commercial Distribution

  • 00195377067067 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x34x24mm 25°
Nuvasive, Inc.
1904425P2
In Commercial Distribution

  • 00195377067050 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x34x24mm 20°
Nuvasive, Inc.
1904420P2
In Commercial Distribution

  • 00195377067043 ()


  • Polymeric spinal interbody fusion cage
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