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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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XLIF - 00887517417220

XLIF Annulus Cutter, 4x16mm Angled
Nuvasive, Inc.
6943416
In Commercial Distribution

  • 00887517417220 ()


  • Orthopaedic implantable-device cutter

XLIF - 00887517417206

XLIF Annulus Cutter, 6x22mm
Nuvasive, Inc.
6942622
In Commercial Distribution

  • 00887517417206 ()


  • Orthopaedic implantable-device cutter

XLIF - 00887517416995

XLIF Annulus Cutter, 6x18mm
Nuvasive, Inc.
6942618
In Commercial Distribution

  • 00887517416995 ()


  • Orthopaedic implantable-device cutter

XLIF - 00887517416964

XLIF Annulus Cutter, 4x22mm
Nuvasive, Inc.
6942422
In Commercial Distribution

  • 00887517416964 ()


  • Orthopaedic implantable-device cutter

XLIF - 00887517416957

XLIF Annulus Cutter, 4x18mm
Nuvasive, Inc.
6942418
In Commercial Distribution

  • 00887517416957 ()


  • Orthopaedic implantable-device cutter

XLIF - 00887517416940

XLIF Annulus Cutter, 4x16mm
Nuvasive, Inc.
6942416
In Commercial Distribution

  • 00887517416940 ()


  • Orthopaedic implantable-device cutter

XLIF - 00887517416926

XLIF Paddle Sizer, 6x22mm Angled
Nuvasive, Inc.
6941622
In Commercial Distribution

  • 00887517416926 ()


  • Spinal implant trial

XLIF - 00887517416575

XLIF Paddle Sizer, 4x18mm Angled
Nuvasive, Inc.
6941418
In Commercial Distribution

  • 00887517416575 ()


  • Spinal implant trial

XLIF - 00887517415868

MaXcess 4 Retractor Level
Nuvasive, Inc.
6940005
In Commercial Distribution

  • 00887517415868 ()


  • Internal spinal fixation procedure kit, reusable

XLIF - 00887517415837

XLIF Slap Hammer
Nuvasive, Inc.
6940002
In Commercial Distribution

  • 00887517415837 ()


  • Internal spinal fixation procedure kit, reusable
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