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 Type Device Class Implantable

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No Description
BIOMET SPINE LLC
8825-0710
In Commercial Distribution

  • 00888480571087 ()

  • ACF PEEK 7°/0° 14X18X10MM
8825-0710

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0709
In Commercial Distribution

  • 00888480571070 ()

  • ACF PEEK 7°/0° 14X18X09MM
8825-0709

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0708
In Commercial Distribution

  • 00888480571063 ()

  • ACF PEEK 7°/0° 14X18X08MM
8825-0708

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0707
In Commercial Distribution

  • 00888480571056 ()

  • ACF PEEK 7°/0° 14X18X07MM
8825-0707

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0706
In Commercial Distribution

  • 00888480571049 ()

  • ACF PEEK 7°/0° 14X18X06MM
8825-0706

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0705
In Commercial Distribution

  • 00888480571032 ()

  • ACF PEEK 7°/0° 14X18X05MM
8825-0705

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0725
In Commercial Distribution

  • 00887868212086 ()

  • VBR PEEK 7°/0° 14x18x25mm
8825-0725

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0724
In Commercial Distribution

  • 00887868212079 ()

  • VBR PEEK 7°/0° 14x18x24mm
8825-0724

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0723
In Commercial Distribution

  • 00887868212062 ()

  • VBR PEEK 7°/0° 14x18x23mm
8825-0723

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0722
In Commercial Distribution

  • 00887868212055 ()

  • VBR PEEK 7°/0° 14x18x22mm
8825-0722

  • Polymeric spinal interbody fusion cage
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