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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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FLXfit 15 Expandable Interbody
CORELINK LLC
AT3212
In Commercial Distribution

  • M725AT32120 ()


  • Metallic spinal interbody fusion cage
FLXfit 15 Expandable Interbody
CORELINK LLC
AT3211
In Commercial Distribution

  • M725AT32110 ()


  • Metallic spinal interbody fusion cage
FLXfit 15 Expandable Interbody
CORELINK LLC
AT3210
In Commercial Distribution

  • M725AT32100 ()


  • Metallic spinal interbody fusion cage
FLXfit 15 Expandable Interbody
CORELINK LLC
AT3209
In Commercial Distribution

  • M725AT32090 ()


  • Metallic spinal interbody fusion cage
FLXfit 15 Expandable Interbody
CORELINK LLC
AT3208
In Commercial Distribution

  • M725AT32080 ()


  • Metallic spinal interbody fusion cage
Lateral Implant, 23mm x 8mm x 60mm, 15 Deg, 3D
Seaspine Orthopedics Corporation
WL4-286015
In Commercial Distribution

  • 10889981330187 ()
WL4-286015

  • Metallic spinal interbody fusion cage
Lateral Implant, 23mm x 8mm x 55mm, 15 Deg, 3D
Seaspine Orthopedics Corporation
WL4-285515
In Commercial Distribution

  • 10889981330163 ()
WL4-285515

  • Metallic spinal interbody fusion cage
Lateral Implant, 23mm x 8mm x 50mm, 15 Deg, 3D
Seaspine Orthopedics Corporation
WL4-285015
In Commercial Distribution

  • 10889981330149 ()
WL4-285015

  • Metallic spinal interbody fusion cage
Lateral Implant, 23mm x 8mm x 45mm, 15 Deg, 3D
Seaspine Orthopedics Corporation
WL4-284515
In Commercial Distribution

  • 10889981330125 ()
WL4-284515

  • Metallic spinal interbody fusion cage
Lateral Implant, 23mm x 8mm x 40mm, 15 Deg, 3D
Seaspine Orthopedics Corporation
WL4-284015
In Commercial Distribution

  • 10889981330101 ()
WL4-284015

  • Metallic spinal interbody fusion cage
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