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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 - 00887517145666

MaXcess MAS TLIF Blade, 60mm C-C Tube
Nuvasive, Inc.
1628283
In Commercial Distribution

  • 00887517145666 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145659

MaXcess MAS TLIF Blade, 50mm C-C Tube
Nuvasive, Inc.
1628282
In Commercial Distribution

  • 00887517145659 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145642

MaXcess MAS TLIF Blade, 40mm C-C Tube
Nuvasive, Inc.
1628281
In Commercial Distribution

  • 00887517145642 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145635

MaXcess MAS TLIF Blade, 120mm C-C
Nuvasive, Inc.
1628269
In Commercial Distribution

  • 00887517145635 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145628

MaXcess MAS TLIF Blade, 110mm C-C
Nuvasive, Inc.
1628268
In Commercial Distribution

  • 00887517145628 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145611

MaXcess MAS TLIF Blade, 100mm C-C
Nuvasive, Inc.
1628267
In Commercial Distribution

  • 00887517145611 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145604

MaXcess MAS TLIF Blade, 90mm C-C
Nuvasive, Inc.
1628266
In Commercial Distribution

  • 00887517145604 ()


  • Surgical retraction system, reusable

MAS PLIF - 00887517145550

MAS PLIF Fixation Loading Block
Nuvasive, Inc.
1581925
In Commercial Distribution

  • 00887517145550 ()


  • Device sterilization/disinfection container, reusable

MaXcess - 00887517145192

MaXcess MAS TLIF Blade, 80mm C-C
Nuvasive, Inc.
1628265
In Commercial Distribution

  • 00887517145192 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145185

MaXcess MAS TLIF Blade, 70mm C-C
Nuvasive, Inc.
1628264
In Commercial Distribution

  • 00887517145185 ()


  • Surgical retraction system, reusable
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