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
8829-2313
In Commercial Distribution

  • 00888480571551 ()

  • PLIF CHANNELED PEEK 0° 10X23X13MM
8829-2313

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2312
In Commercial Distribution

  • 00888480571544 ()

  • PLIF CHANNELED PEEK 0° 10X23X12MM
8829-2312

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2311
In Commercial Distribution

  • 00888480571537 ()

  • PLIF CHANNELED PEEK 0° 10X23X11MM
8829-2311

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2310
In Commercial Distribution

  • 00888480571520 ()

  • PLIF CHANNELED PEEK 0° 10X23X10MM
8829-2310

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2309
In Commercial Distribution

  • 00888480571513 ()

  • PLIF CHANNELED PEEK 0° 10X23X9MM
8829-2309

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2308
In Commercial Distribution

  • 00888480571506 ()

  • PLIF CHANNELED PEEK 0° 10X23X8MM
8829-2308

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8829-2307
In Commercial Distribution

  • 00888480571490 ()

  • PLIF CHANNELED PEEK 0° 10X23X7MM
8829-2307

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0750
In Commercial Distribution

  • 00888480571483 ()

  • VBR PEEK 7°/0° 14X18X50MM
8825-0750

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0749
In Commercial Distribution

  • 00888480571476 ()

  • VBR PEEK 7°/0° 14X18X49MM
8825-0749

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0748
In Commercial Distribution

  • 00888480571469 ()

  • VBR PEEK 7°/0° 14X18X48MM
8825-0748

  • Polymeric spinal interbody fusion cage
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