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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 Type Device Class Implantable

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Timberline® Lateral Interbody Fusion System - 00887868203725

No Description
BIOMET SPINE LLC
8708-6050
In Commercial Distribution

  • 00887868203725 ()

  • Spacer Lat PEEK 8° CT 60L X 26W X 50H
8708-6050

  • Polymeric spinal interbody fusion cage

Timberline® Lateral Interbody Fusion System - 00887868203718

No Description
BIOMET SPINE LLC
8708-6045
In Commercial Distribution

  • 00887868203718 ()

  • Spacer Lat PEEK 8° CT 60L X 26W X 45H
8708-6045

  • Polymeric spinal interbody fusion cage

Timberline® Lateral Interbody Fusion System - 00887868203695

No Description
BIOMET SPINE LLC
8708-6035
In Commercial Distribution

  • 00887868203695 ()

  • Spacer Lat PEEK 8° CT 60L X 26W X 35H
8708-6035

  • Polymeric spinal interbody fusion cage

Timberline® Lateral Interbody Fusion System - 00887868203664

No Description
BIOMET SPINE LLC
8708-6020
In Commercial Distribution

  • 00887868203664 ()

  • Spacer Lat PEEK 8° CT 60L X 26W X 20H
8708-6020

  • Polymeric spinal interbody fusion cage

Timberline® Lateral Interbody Fusion System - 00887868203640

No Description
BIOMET SPINE LLC
8708-6016
In Commercial Distribution

  • 00887868203640 ()

  • Spacer Lat PEEK 8° CT 60L X 26W X 16H
8708-6016

  • Polymeric spinal interbody fusion cage

Timberline® Lateral Interbody Fusion System - 00887868203626

No Description
BIOMET SPINE LLC
8708-6012
In Commercial Distribution

  • 00887868203626 ()

  • Spacer Lat PEEK 8° CT 60L X 26W X 12H
8708-6012

  • Polymeric spinal interbody fusion cage

Timberline® Lateral Interbody Fusion System - 00887868203602

No Description
BIOMET SPINE LLC
8708-5550
In Commercial Distribution

  • 00887868203602 ()

  • Spacer Lat PEEK 8° CT 55L X 26W X 50H
8708-5550

  • Polymeric spinal interbody fusion cage

Timberline® Lateral Interbody Fusion System - 00887868203589

No Description
BIOMET SPINE LLC
8708-5540
In Commercial Distribution

  • 00887868203589 ()

  • Spacer Lat PEEK 8° CT 55L X 26W X 40H
8708-5540

  • Polymeric spinal interbody fusion cage

Timberline® Lateral Interbody Fusion System - 00887868203565

No Description
BIOMET SPINE LLC
8708-5530
In Commercial Distribution

  • 00887868203565 ()

  • Spacer Lat PEEK 8° CT 55L X 26W X 30H
8708-5530

  • Polymeric spinal interbody fusion cage

Timberline® Lateral Interbody Fusion System - 00887868203541

No Description
BIOMET SPINE LLC
8708-5520
In Commercial Distribution

  • 00887868203541 ()

  • Spacer Lat PEEK 8° CT 55L X 26W X 20H
8708-5520

  • Polymeric spinal interbody fusion cage
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