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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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Interlock II, 7x17x14mm 7° Contoured MI
Nuvasive, Inc.
6775707
In Commercial Distribution

  • 00887517810458 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 6x17x14mm 7° Contoured MI
Nuvasive, Inc.
6775706
In Commercial Distribution

  • 00887517810434 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 5x17x14mm 7° Contoured MI
Nuvasive, Inc.
6775705
In Commercial Distribution

  • 00887517810410 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 16x17x14mm 30°
Nuvasive, Inc.
6771630
In Commercial Distribution

  • 00887517810397 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 16x17x14mm 25°
Nuvasive, Inc.
6771625
In Commercial Distribution

  • 00887517810373 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 16x17x14mm 20°
Nuvasive, Inc.
6771620
In Commercial Distribution

  • 00887517810359 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 16x17x14mm 15°
Nuvasive, Inc.
6771615
In Commercial Distribution

  • 00887517810335 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 16x17x14mm 10°
Nuvasive, Inc.
6771610
In Commercial Distribution

  • 00887517810311 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 16x17x14mm 7°
Nuvasive, Inc.
6771607
In Commercial Distribution

  • 00887517810298 ()


  • Polymeric spinal interbody fusion cage
Interlock II, 15x17x14mm 30°
Nuvasive, Inc.
6771530
In Commercial Distribution

  • 00887517810274 ()


  • Polymeric spinal interbody fusion cage
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