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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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Traverse - 00887517151841

Traverse Plate, Size 20 Fixed
Nuvasive, Inc.
7820020
In Commercial Distribution

  • 00887517151841 ()


  • Spinal fixation plate, non-bioabsorbable

TRUELOK SYSTEM - 18033509853524

TL,BOLT, 12MM, QTY. 20
ORTHOFIX SRL
1
In Commercial Distribution

  • 18033509853524 ()

  • Width: 129 Millimeter
54-1050M

  • External orthopaedic fixation system, single-use

TRUELOK SYSTEM - 18033509853500

TL,BOLT, 16MM, QTY. 20
ORTHOFIX SRL
1
In Commercial Distribution

  • 18033509853500 ()

  • Width: 127 Millimeter
54-1010M

  • External orthopaedic fixation system, single-use

Triad - 00887517057129

Triad TLIF Distractor, 20° Bend
Nuvasive, Inc.
1008044
In Commercial Distribution

  • 00887517057129 ()


  • Implantable craniofacial bone distractor

CoRoent - 00887517296221

CoRoent® XL-H, 10x22x60mm 20°
Nuvasive, Inc.
6201060
In Commercial Distribution

  • 00887517296221 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517296214

CoRoent® XL-H, 10x22x55mm 20°
Nuvasive, Inc.
6201055
In Commercial Distribution

  • 00887517296214 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517296207

CoRoent® XL-H, 10x22x50mm 20°
Nuvasive, Inc.
6201050
In Commercial Distribution

  • 00887517296207 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517295897

CoRoent® XL-H, 10x22x45mm 20°
Nuvasive, Inc.
6201045
In Commercial Distribution

  • 00887517295897 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517295859

CoRoent® XL-H, 8x22x60mm 20°
Nuvasive, Inc.
6200860
In Commercial Distribution

  • 00887517295859 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517295842

CoRoent® XL-H, 8x22x55mm 20°
Nuvasive, Inc.
6200855
In Commercial Distribution

  • 00887517295842 ()


  • Metallic spinal interbody fusion cage
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