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
8880-0210
In Commercial Distribution

  • 00888480572619 ()

  • ALIF PEEK 0° 27X36X10MM
8880-0210

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0208
In Commercial Distribution

  • 00888480572602 ()

  • ALIF PEEK 0° 27X36X8MM
8880-0208

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0120
In Commercial Distribution

  • 00888480572596 ()

  • ALIF PEEK 0° 24X32X20MM
8880-0120

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0118
In Commercial Distribution

  • 00888480572589 ()

  • ALIF PEEK 0° 24X32X18MM
8880-0118

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0116
In Commercial Distribution

  • 00888480572572 ()

  • ALIF PEEK 0° 24X32X16MM
8880-0116

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0114
In Commercial Distribution

  • 00888480572565 ()

  • ALIF PEEK 0° 24X32X14MM
8880-0114

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0112
In Commercial Distribution

  • 00888480572558 ()

  • ALIF PEEK 0° 24X32X12MM
8880-0112

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0110
In Commercial Distribution

  • 00888480572541 ()

  • ALIF PEEK 0° 24X32X10MM
8880-0110

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0108
In Commercial Distribution

  • 00888480572534 ()

  • ALIF PEEK 0° 24X32X8MM
8880-0108

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-4412
In Commercial Distribution

  • 00888480570707 ()

  • ACDF PEEK 0° 15X20X12MM
8824-4412

  • Polymeric spinal interbody fusion cage
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