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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 Class Implantable

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CoRoent - 00887517401298

Oblique TLIF, 12x10x30mm 5°
Nuvasive, Inc.
1659146
In Commercial Distribution

  • 00887517401298 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517401250

Oblique TLIF, 8x10x30mm 5°
Nuvasive, Inc.
1659142
In Commercial Distribution

  • 00887517401250 ()


  • Polymeric spinal interbody fusion cage

VuePoint - 00887517400994

VuePoint® II Screw, 4.5x38mm MA
Nuvasive, Inc.
8975738
In Commercial Distribution

  • 00887517400994 ()


  • Bone-screw internal spinal fixation system, non-sterile

VuePoint - 00887517400598

VuePoint® II Screw, 4.5x18mm MA
Nuvasive, Inc.
8975718
In Commercial Distribution

  • 00887517400598 ()


  • Bone-screw internal spinal fixation system, non-sterile

VuePoint - 00887517400581

VuePoint® II Screw, 4.5x16mm MA
Nuvasive, Inc.
8975716
In Commercial Distribution

  • 00887517400581 ()


  • Bone-screw internal spinal fixation system, non-sterile

VuePoint - 00887517400574

VuePoint® II Screw, 4.5x14mm MA
Nuvasive, Inc.
8975714
In Commercial Distribution

  • 00887517400574 ()


  • Bone-screw internal spinal fixation system, non-sterile

VuePoint - 00887517400567

VuePoint® II Screw, 4.5x12mm MA
Nuvasive, Inc.
8975712
In Commercial Distribution

  • 00887517400567 ()


  • Bone-screw internal spinal fixation system, non-sterile

VuePoint - 00887517400550

VuePoint® II Screw, 4.5x10mm MA
Nuvasive, Inc.
8975710
In Commercial Distribution

  • 00887517400550 ()


  • Bone-screw internal spinal fixation system, non-sterile

CoRoent - 00887517400031

CoRoent XL, 10X18x50mm 8°
Nuvasive, Inc.
6951050
In Commercial Distribution

  • 00887517400031 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517399779

CoRoent® XLR, 20x34x24 12°
Nuvasive, Inc.
6942044
In Commercial Distribution

  • 00887517399779 ()


  • Polymeric spinal interbody fusion cage
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