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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 Size Device Size Type Device Class Implantable

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MaXcess - 00887517499592

MaXcess MAS TLIF Blade, 70mm Left C-C
Nuvasive, Inc.
1684304
In Commercial Distribution

  • 00887517499592 ()


  • Surgical retraction system, reusable

MaXcess - 00887517499578

MaXcess MAS TLIF Blade, 50mm Left C-C
Nuvasive, Inc.
1684302
In Commercial Distribution

  • 00887517499578 ()


  • Surgical retraction system, reusable

MaXcess - 00887517514028

MaXcess MAS TLIF Blade, 100mm Left C-C
Nuvasive, Inc.
1684307
In Commercial Distribution

  • 00887517514028 ()


  • Surgical retraction system, reusable

MaXcess - 00887517514011

MaXcess MAS TLIF Blade, 90mm Left C-C
Nuvasive, Inc.
1684306
In Commercial Distribution

  • 00887517514011 ()


  • Surgical retraction system, reusable

MaXcess - 00887517514004

MaXcess MAS TLIF Blade, 80mm Left C-C
Nuvasive, Inc.
1684305
In Commercial Distribution

  • 00887517514004 ()


  • Surgical retraction system, reusable

MaXcess - 00887517146120

MaXcess MAS TLIF Blade, 120mm C-C Tube
Nuvasive, Inc.
1628289
In Commercial Distribution

  • 00887517146120 ()


  • Surgical retraction system, reusable

MaXcess - 00887517146113

MaXcess MAS TLIF Blade, 110mm C-C Tube
Nuvasive, Inc.
1628288
In Commercial Distribution

  • 00887517146113 ()


  • Surgical retraction system, reusable

MaXcess - 00887517146106

MaXcess MAS TLIF Blade, 100mm C-C Tube
Nuvasive, Inc.
1628287
In Commercial Distribution

  • 00887517146106 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145680

MaXcess MAS TLIF Blade, 80mm C-C Tube
Nuvasive, Inc.
1628285
In Commercial Distribution

  • 00887517145680 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145673

MaXcess MAS TLIF Blade, 70mm C-C Tube
Nuvasive, Inc.
1628284
In Commercial Distribution

  • 00887517145673 ()


  • Surgical retraction system, reusable
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