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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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Camber - 00887517995773

Camber Trad Plate, 14mm Lg Lamina C-C
Nuvasive, Inc.
8370020P
In Commercial Distribution

  • 00887517995773 ()


  • Spinal fixation plate, non-bioabsorbable

Camber - 00887517995766

Camber Trad Plate, 12mm Lg Lamina C-C
Nuvasive, Inc.
8370019P
In Commercial Distribution

  • 00887517995766 ()


  • Spinal fixation plate, non-bioabsorbable

Camber - 00887517995759

Camber Trad Plate, 10mm Lg Lamina C-C
Nuvasive, Inc.
8370018P
In Commercial Distribution

  • 00887517995759 ()


  • Spinal fixation plate, non-bioabsorbable

Camber - 00887517995742

Camber Trad Plate, 8mm Lg Lamina C-C
Nuvasive, Inc.
8370017P
In Commercial Distribution

  • 00887517995742 ()


  • Spinal fixation plate, non-bioabsorbable

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 - 00887517145697

MaXcess MAS TLIF Blade, 90mm C-C Tube
Nuvasive, Inc.
1628286
In Commercial Distribution

  • 00887517145697 ()


  • 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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