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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, 8x34x24mm 25°
Nuvasive, Inc.
1984425P2
In Commercial Distribution

  • 00195377067586 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x34x24mm 20°
Nuvasive, Inc.
1984420P2
In Commercial Distribution

  • 00195377067579 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x34x24mm 15°
Nuvasive, Inc.
1984415P2
In Commercial Distribution

  • 00195377067562 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x34x24mm 10°
Nuvasive, Inc.
1984410P2
In Commercial Distribution

  • 00195377067555 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x42x32mm 30°
Nuvasive, Inc.
1982030P2
In Commercial Distribution

  • 00195377067548 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x42x32mm 25°
Nuvasive, Inc.
1982025P2
In Commercial Distribution

  • 00195377067531 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x42x32mm 20°
Nuvasive, Inc.
1982020P2
In Commercial Distribution

  • 00195377067524 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x42x32mm 15°
Nuvasive, Inc.
1982015P2
In Commercial Distribution

  • 00195377067517 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x42x32mm 10°
Nuvasive, Inc.
1982010P2
In Commercial Distribution

  • 00195377067500 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 7x26x22mm 20°
Nuvasive, Inc.
1976220P2
In Commercial Distribution

  • 00195377067494 ()


  • Polymeric spinal interbody fusion cage
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