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

  • 00887517145628 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 100mm C-C
Nuvasive, Inc.
1628267
In Commercial Distribution

  • 00887517145611 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 90mm C-C
Nuvasive, Inc.
1628266
In Commercial Distribution

  • 00887517145604 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 80mm C-C
Nuvasive, Inc.
1628265
In Commercial Distribution

  • 00887517145192 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 70mm C-C
Nuvasive, Inc.
1628264
In Commercial Distribution

  • 00887517145185 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 60mm C-C
Nuvasive, Inc.
1628263
In Commercial Distribution

  • 00887517145178 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 50mm C-C
Nuvasive, Inc.
1628262
In Commercial Distribution

  • 00887517145161 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 40mm C-C
Nuvasive, Inc.
1628261
In Commercial Distribution

  • 00887517145154 ()


  • Surgical retraction system, reusable
BLADE X07317191 SLIM CC L 190MM
MEDTRONIC SOFAMOR DANEK, INC.
X07317191
In Commercial Distribution

  • 00763000897185 ()


  • Surgical retraction system, reusable
BLADE X07317190 SLIM CC R 190MM
MEDTRONIC SOFAMOR DANEK, INC.
X07317190
In Commercial Distribution

  • 00763000897178 ()


  • Surgical retraction system, reusable
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