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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COHERE TLIF-A, 12x11x30mm 8°
Nuvasive, Inc.
4121308P2
In Commercial Distribution

  • 00887517022059 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-A, 11x9x30mm 8°
Nuvasive, Inc.
4119308P2
In Commercial Distribution

  • 00887517022035 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-A, 11x11x30mm 8°
Nuvasive, Inc.
4111308P2
In Commercial Distribution

  • 00887517022011 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 14x10x30mm 4°
Nuvasive, Inc.
6140304P2
In Commercial Distribution

  • 00887517020857 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 14x10x25mm 4°
Nuvasive, Inc.
6140254P2
In Commercial Distribution

  • 00887517020833 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 12x10x35mm 4°
Nuvasive, Inc.
6120354P2
In Commercial Distribution

  • 00887517020819 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 12x10x30mm 4°
Nuvasive, Inc.
6120304P2
In Commercial Distribution

  • 00887517020802 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 12x10x30mm 12°
Nuvasive, Inc.
6120302P2
In Commercial Distribution

  • 00887517020796 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 12x10x25mm 4°
Nuvasive, Inc.
6120254P2
In Commercial Distribution

  • 00887517020789 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 12x10x25mm 12°
Nuvasive, Inc.
6120252P2
In Commercial Distribution

  • 00887517020772 ()


  • Polymeric spinal interbody fusion cage
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