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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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C-C Blade, Right 80mm, Ø22
K2M, INC.
8030-90017
In Commercial Distribution

  • 10888857553644 ()
8030-90017

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 220mm, Ø22
K2M, INC.
8030-90016
In Commercial Distribution

  • 10888857553637 ()
8030-90016

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 210mm, Ø22
K2M, INC.
8030-90015
In Commercial Distribution

  • 10888857553620 ()
8030-90015

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 200mm, Ø22
K2M, INC.
8030-90014
In Commercial Distribution

  • 10888857553613 ()
8030-90014

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 190mm, Ø22
K2M, INC.
8030-90013
In Commercial Distribution

  • 10888857553606 ()
8030-90013

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 180mm, Ø22
K2M, INC.
8030-90012
In Commercial Distribution

  • 10888857553590 ()
8030-90012

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 170mm, Ø22
K2M, INC.
8030-90011
In Commercial Distribution

  • 10888857553583 ()
8030-90011

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 160mm, Ø22
K2M, INC.
8030-90010
In Commercial Distribution

  • 10888857553576 ()
8030-90010

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 150mm, Ø22
K2M, INC.
8030-90009
In Commercial Distribution

  • 10888857553569 ()
8030-90009

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 140mm, Ø22
K2M, INC.
8030-90008
In Commercial Distribution

  • 10888857553552 ()
8030-90008

  • Surgical retractor/retraction system blade, reusable
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