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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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MaXcess - 00887517143037

MaXcess MAS PLIF Blade, 60mm Lft Narrow
Nuvasive, Inc.
1579762
In Commercial Distribution

  • 00887517143037 ()


  • Surgical retraction system, reusable

MaXcess - 00887517143013

MaXcess MAS PLIF Blade, 90mm Lft Wide
Nuvasive, Inc.
1579745
In Commercial Distribution

  • 00887517143013 ()


  • Surgical retraction system, reusable

MaXcess - 00887517142597

MaXcess MAS PLIF Blade, 70mm Lft Wide
Nuvasive, Inc.
1579743
In Commercial Distribution

  • 00887517142597 ()


  • Surgical retraction system, reusable

MaXcess - 00887517142573

MaXcess MAS PLIF Blade, 50mm Lft Wide
Nuvasive, Inc.
1579741
In Commercial Distribution

  • 00887517142573 ()


  • Surgical retraction system, reusable

MaXcess - 00887517142559

MaXcess MAS PLIF Blade, 80mm Rt Narrow
Nuvasive, Inc.
1579724
In Commercial Distribution

  • 00887517142559 ()


  • Surgical retraction system, reusable

MaXcess - 00887517142535

MaXcess MAS PLIF Blade, 60mm Rt Narrow
Nuvasive, Inc.
1579722
In Commercial Distribution

  • 00887517142535 ()


  • Surgical retraction system, reusable

MaXcess - 00887517142511

MaXcess MAS PLIF Blade, 90mm Rt Wide
Nuvasive, Inc.
1579685
In Commercial Distribution

  • 00887517142511 ()


  • Surgical retraction system, reusable

XLIF - 00887517142177

XLIF Cutter, 6x18mm Annulus Angled
Nuvasive, Inc.
1593363
In Commercial Distribution

  • 00887517142177 ()


  • Orthopaedic implantable-device cutter

XLIF - 00887517142153

XLIF Cutter, 4x14mm Annulus
Nuvasive, Inc.
1593361
In Commercial Distribution

  • 00887517142153 ()


  • Orthopaedic implantable-device cutter

XLIF - 00887517142139

XLIF Rasp, Angled
Nuvasive, Inc.
1593341
In Commercial Distribution

  • 00887517142139 ()


  • Bone file/rasp, manual, reusable
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