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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BLADE X07317190 SLIM CC R 190MM
MEDTRONIC SOFAMOR DANEK, INC.
X07317190
In Commercial Distribution

  • 00763000897178 ()


  • Surgical retraction system, reusable
BLADE X07317151 SLIM CC L 150MM
MEDTRONIC SOFAMOR DANEK, INC.
X07317151
In Commercial Distribution

  • 00763000897123 ()


  • Surgical retraction system, reusable
BLADE X07317130 SLIM CC R 130MM
MEDTRONIC SOFAMOR DANEK, INC.
X07317130
In Commercial Distribution

  • 00763000897086 ()


  • Surgical retraction system, reusable
BLADE X07317111 SLIM CC L 110MM
MEDTRONIC SOFAMOR DANEK, INC.
X07317111
In Commercial Distribution

  • 00763000897062 ()


  • Surgical retraction system, reusable
BLADE X07317091 SLIM CC L 90MM
MEDTRONIC SOFAMOR DANEK, INC.
X07317091
In Commercial Distribution

  • 00763000897031 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 120mm C-C
Nuvasive, Inc.
1628269
In Commercial Distribution

  • 00887517145635 ()


  • Surgical retraction system, reusable
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
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