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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 - 00887517650351

MaXcess MAS TLIF Blade, 110mm Right Tube
Nuvasive, Inc.
3500308
In Commercial Distribution

  • 00887517650351 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650344

MaXcess MAS TLIF Blade, 100mm Right Tube
Nuvasive, Inc.
3500307
In Commercial Distribution

  • 00887517650344 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650337

MaXcess MAS TLIF Blade, 90mm Right Tube
Nuvasive, Inc.
3500306
In Commercial Distribution

  • 00887517650337 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650320

MaXcess MAS TLIF Blade, 80mm Right Tube
Nuvasive, Inc.
3500305
In Commercial Distribution

  • 00887517650320 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650313

MaXcess MAS TLIF Blade, 70mm Right Tube
Nuvasive, Inc.
3500304
In Commercial Distribution

  • 00887517650313 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650306

MaXcess MAS TLIF Blade, 60mm Right Tube
Nuvasive, Inc.
3500303
In Commercial Distribution

  • 00887517650306 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650290

MaXcess MAS TLIF Blade, 50mm Right Tube
Nuvasive, Inc.
3500302
In Commercial Distribution

  • 00887517650290 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650283

MaXcess MAS TLIF Blade, 40mm Right Tube
Nuvasive, Inc.
3500301
In Commercial Distribution

  • 00887517650283 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650276

MaXcess MAS TLIF Blade, 150mm Left Tube
Nuvasive, Inc.
3500212
In Commercial Distribution

  • 00887517650276 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650269

MaXcess MAS TLIF Blade, 140mm Left Tube
Nuvasive, Inc.
3500211
In Commercial Distribution

  • 00887517650269 ()


  • Surgical retraction system, reusable
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