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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 - 00887517175922

MaXcess Micro-Decompression Woodson
Nuvasive, Inc.
3100130
In Commercial Distribution

  • 00887517175922 ()


  • Surgical retraction system, reusable

MaXcess - 00887517175915

MAS Micro-Decomp Curette, Rev Ang Sm
Nuvasive, Inc.
3100128
In Commercial Distribution

  • 00887517175915 ()


  • Neurosurgical curette, single-use

MaXcess - 00887517174390

MAS Micro-Decomp Curette, Rev Ang Lg
Nuvasive, Inc.
3100126
In Commercial Distribution

  • 00887517174390 ()


  • Neurosurgical curette, single-use

MaXcess - 00887517174376

MAS Micro-Decomp Curette, Ang Med
Nuvasive, Inc.
3100124
In Commercial Distribution

  • 00887517174376 ()


  • Neurosurgical curette, single-use

MaXcess - 00887517174369

MAS Micro-Decomp Curette, Ang Lg
Nuvasive, Inc.
3100123
In Commercial Distribution

  • 00887517174369 ()


  • Neurosurgical curette, single-use

MaXcess - 00887517174345

MAS Micro Decomp Curette, Straight Med
Nuvasive, Inc.
3100121
In Commercial Distribution

  • 00887517174345 ()


  • Neurosurgical curette, single-use

MaXcess - 00887517174321

MaXcess Micro Decomp Kerrison, 2mm 90°
Nuvasive, Inc.
3100103
In Commercial Distribution

  • 00887517174321 ()


  • Surgical retraction system, reusable

MaXcess - 00887517174314

MaXcess Micro Decomp Kerrison, 1mm 90°
Nuvasive, Inc.
3100102
In Commercial Distribution

  • 00887517174314 ()


  • Surgical retraction system, reusable

MaXcess - 00887517174307

MaXcess Micro Decomp Kerrison, 2mm 40°
Nuvasive, Inc.
3100101
In Commercial Distribution

  • 00887517174307 ()


  • Surgical retraction system, reusable

VuePoint - 00887517173232

VuePoint Drill Bit, 2.05mm
Nuvasive, Inc.
7901091
In Commercial Distribution

  • 00887517173232 ()


  • Internal spinal fixation procedure kit, single-use
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