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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 210mm, Ø22
K2M, INC.
8030-90030
In Commercial Distribution

  • 10888857553774 ()
8030-90030

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 200mm, Ø22
K2M, INC.
8030-90029
In Commercial Distribution

  • 10888857553767 ()
8030-90029

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 190mm, Ø22
K2M, INC.
8030-90028
In Commercial Distribution

  • 10888857553750 ()
8030-90028

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 180mm, Ø22
K2M, INC.
8030-90027
In Commercial Distribution

  • 10888857553743 ()
8030-90027

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 170mm, Ø22
K2M, INC.
8030-90026
In Commercial Distribution

  • 10888857553736 ()
8030-90026

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 160mm, Ø22
K2M, INC.
8030-90025
In Commercial Distribution

  • 10888857553729 ()
8030-90025

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 150mm, Ø22
K2M, INC.
8030-90024
In Commercial Distribution

  • 10888857553712 ()
8030-90024

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 140mm, Ø22
K2M, INC.
8030-90023
In Commercial Distribution

  • 10888857553705 ()
8030-90023

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 130mm, Ø22
K2M, INC.
8030-90022
In Commercial Distribution

  • 10888857553699 ()
8030-90022

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 120mm, Ø22
K2M, INC.
8030-90021
In Commercial Distribution

  • 10888857553682 ()
8030-90021

  • Surgical retractor/retraction system blade, reusable
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