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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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PEEK/Titanium Interbody, 12 °, 42mm x 30mm
Altus Spine, LLC
SL42301217
In Commercial Distribution

  • 00843210159256 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 42mmx30mm
Altus Spine, LLC
SL42302017T
In Commercial Distribution

  • 00843210180168 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 42mmx30mm
Altus Spine, LLC
SL42302018T
In Commercial Distribution

  • 00843210180151 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 42mmx30mm
Altus Spine, LLC
SL42302019T
In Commercial Distribution

  • 00843210180144 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 42mmx30mm
Altus Spine, LLC
SL42302020T
In Commercial Distribution

  • 00843210180137 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 25 degree, 42mmx30mm
Altus Spine, LLC
SL42302517T
In Commercial Distribution

  • 00843210180120 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 25 degree, 42mmx30mm
Altus Spine, LLC
SL42302518T
In Commercial Distribution

  • 00843210180113 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 25 degree, 42mmx30mm
Altus Spine, LLC
SL42302519T
In Commercial Distribution

  • 00843210180106 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 25 degree, 42mmx30mm
Altus Spine, LLC
SL42302520T
In Commercial Distribution

  • 00843210180090 ()


  • Polymeric spinal interbody fusion cage
Implant Bar Inserter
Altus Spine, LLC
1030-0001
In Commercial Distribution

  • 00843210179797 ()


  • Polymeric spinal interbody fusion cage
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