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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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Bone Awl (retracting) - M739CP50100

No Description
CAPTIVA SPINE, INC.
CP50100
In Commercial Distribution

  • M739CP50100 ()


  • Bone awl, reusable

Rampart One Lumbar Interbody Fusion System - M7401001294

325mm Handheld Straight Awl
SPINEOLOGY INC.
102-56-01
In Commercial Distribution

  • M7401001294 ()
100-1294

  • Bone awl, reusable

Rampart One Lumbar Interbody Fusion System - M7401001293

Straight Awl
SPINEOLOGY INC.
102-55-01
In Commercial Distribution

  • M7401001293 ()
100-1293

  • Bone awl, reusable

Threshold Pedicular Fixation System - M7405530020

Awl
SPINEOLOGY INC.
10-62-01
In Commercial Distribution

  • M7405530020 ()
553-0020

  • Bone awl, reusable

Threshold Pedicular Fixation System - M7405300005

AWL Handle
SPINEOLOGY INC.
53-07-30
In Commercial Distribution

  • M7405300005 ()
530-0005

  • Bone awl, reusable

Threshold Pedicular Fixation System - M7405300004

AWL Cap
SPINEOLOGY INC.
53-07-29
In Commercial Distribution

  • M7405300004 ()
530-0004

  • Bone awl, reusable

Threshold Pedicular Fixation System - M7405300003

AWL Stylet
SPINEOLOGY INC.
53-07-33
In Commercial Distribution

  • M7405300003 ()
530-0003

  • Bone awl, reusable

Threshold Pedicular Fixation System - M7405300002

Cannulated AWL Shaft
SPINEOLOGY INC.
53-07-07
In Commercial Distribution

  • M7405300002 ()
530-0002

  • Bone awl, reusable

Rampart One Lumbar Interbody Fusion System - M7404900009

Handheld Variable Angle Awl
SPINEOLOGY INC.
49-01-75
In Commercial Distribution

  • M7404900009 ()
490-0009

  • Bone awl, reusable

Rampart One Lumbar Interbody Fusion System - M7404900007

Sleeved Punch Awl
SPINEOLOGY INC.
49-01-70
In Commercial Distribution

  • M7404900007 ()
490-0007

  • Bone awl, reusable
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