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 LO Titanium, 9x10x40 5°
Nuvasive, Inc.
6080940P
In Commercial Distribution

  • 00887517032492 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 9x10x35 5°
Nuvasive, Inc.
6080935P
In Commercial Distribution

  • 00887517032485 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 9x10x30 5°
Nuvasive, Inc.
6080930P
In Commercial Distribution

  • 00887517032478 ()


  • Metallic spinal interbody fusion cage
RELINE-O X-Conn, 30mm 5.0 Rod Fixed
Nuvasive, Inc.
10050330P
In Commercial Distribution

  • 00887517030795 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O X-Conn, 27.5mm 5.0 Rod Fixed
Nuvasive, Inc.
10050327P
In Commercial Distribution

  • 00887517030788 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O X-Conn, 22.5mm 5.0 Rod Fixed
Nuvasive, Inc.
10050322P
In Commercial Distribution

  • 00887517030771 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O X-Conn, 20mm 5.0 Rod Fixed
Nuvasive, Inc.
10050320P
In Commercial Distribution

  • 00887517030764 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Rod Template, Single Level
Nuvasive, Inc.
10000841P
In Commercial Distribution

  • 00887517030757 ()


  • Internal spinal fixation procedure kit, single-use
RELINE-O Rod Template, Multilevel
Nuvasive, Inc.
10000840P
In Commercial Distribution

  • 00887517030740 ()


  • Internal spinal fixation procedure kit, single-use
COHERE TLIF-A, 14x11x34mm 8°
Nuvasive, Inc.
4141348P2
In Commercial Distribution

  • 00887517022141 ()


  • Polymeric spinal interbody fusion cage
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